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4248-19-5 Usage

Uses

tert-Butyl carbamate was used in palladium-catalyzed synthesis of N-Boc-protected anilines. It was used in the synthesis of tetrasubstituted pyrroles, functionalized with ester or ketone groups at C-3 position.

Synthesis Reference(s)

The Journal of Organic Chemistry, 28, p. 3421, 1963 DOI: 10.1021/jo01047a033

General Description

Palladium-catalyzed cross-coupling reaction of tert-butyl carbamate with various aryl(Het) halides with Cs2CO3 as base in 1,4-dioxane (solvent) has been investigated.

Check Digit Verification of cas no

The CAS Registry Mumber 4248-19-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,4 and 8 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 4248-19:
(6*4)+(5*2)+(4*4)+(3*8)+(2*1)+(1*9)=85
85 % 10 = 5
So 4248-19-5 is a valid CAS Registry Number.
InChI:InChI=1/C5H11NO2/c1-5(2,3)8-4(6)7/h1-3H3,(H2,6,7)

4248-19-5 Well-known Company Product Price

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  • Alfa Aesar

  • (L00259)  tert-Butyl carbamate, 98+%   

  • 4248-19-5

  • 1g

  • 152.0CNY

  • Detail
  • Alfa Aesar

  • (L00259)  tert-Butyl carbamate, 98+%   

  • 4248-19-5

  • 5g

  • 425.0CNY

  • Detail
  • Alfa Aesar

  • (L00259)  tert-Butyl carbamate, 98+%   

  • 4248-19-5

  • 25g

  • 1608.0CNY

  • Detail
  • Aldrich

  • (167398)  tert-Butylcarbamate  98%

  • 4248-19-5

  • 167398-1G

  • 152.10CNY

  • Detail
  • Aldrich

  • (167398)  tert-Butylcarbamate  98%

  • 4248-19-5

  • 167398-5G

  • 284.31CNY

  • Detail
  • Aldrich

  • (167398)  tert-Butylcarbamate  98%

  • 4248-19-5

  • 167398-25G

  • 875.16CNY

  • Detail
  • Aldrich

  • (167398)  tert-Butylcarbamate  98%

  • 4248-19-5

  • 167398-100G

  • 1,709.37CNY

  • Detail

4248-19-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name tert-Butyl carbamate

1.2 Other means of identification

Product number -
Other names BOC-AMIDE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:4248-19-5 SDS

4248-19-5Synthetic route

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With ammonia In ethanol at 0 - 20℃;98%
With ammonium hydroxide In ethanol; water at -10 - 20℃; for 18.5833h;95%
With ammonia In methanol at 0 - 20℃; for 7h;94%
urea
57-13-6

urea

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With merrifield anchored iron(II)-anthra catalyst In 1,4-dioxane at 120℃; for 6.5h;81%
With cholin chloride ZnCl2; iron oxide at 130℃; for 6h; Green chemistry;69%
1,2-bis(1-isocyanato-1-methylethyl)diazene
70678-13-6

1,2-bis(1-isocyanato-1-methylethyl)diazene

tert-butyl alcohol
75-65-0

tert-butyl alcohol

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

5,5-dimethyl-Δ1-1,2,4-triazolin-3-one
112700-85-3

5,5-dimethyl-Δ1-1,2,4-triazolin-3-one

Conditions
ConditionsYield
for 22h; Heating;A 29%
B 74%
sodium isocyanate
917-61-3

sodium isocyanate

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With perchloric acid on silica gel at 20℃; for 0.75h;74%
With trifluoroacetic acid 2.) CH2Cl2; Multistep reaction;
(4-aminotetrahydrofuran-3-yl)carbamic acid tert-butyl ester
1330763-30-8

(4-aminotetrahydrofuran-3-yl)carbamic acid tert-butyl ester

4-[(4-fluorophenyl)methyl]-cyclohexanone
335276-54-5

4-[(4-fluorophenyl)methyl]-cyclohexanone

A

tert-butyl (3S,4S)-4-{[4-(4-fluorobenzyl)cyclohexyl]amino}tetrahydro-3-furanylcarbamate
335388-53-9

tert-butyl (3S,4S)-4-{[4-(4-fluorobenzyl)cyclohexyl]amino}tetrahydro-3-furanylcarbamate

B

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With sodium tris(acetoxy)borohydride In methanol; dichloromethane; 1,2-dichloro-ethaneA 53%
B n/a
potassium cyanate
590-28-3

potassium cyanate

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With para-dodecylbenzenesulfonic acid In neat (no solvent) at 60℃; for 0.5h; Green chemistry;52%
With DBSA at 60℃; for 1h;
With DBSA at 60℃; for 1h;
With DBSA at 60℃; for 1h;
Methyl 3-aminothiophene-2-carboxylate
22288-78-4

Methyl 3-aminothiophene-2-carboxylate

di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With dmap In hexane; dichloromethane; ethyl acetate36%
Boc-Lys-NH2 hemioxalate
85535-53-1

Boc-Lys-NH2 hemioxalate

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

6-aminocaproic amide
373-04-6

6-aminocaproic amide

C

tert-butyl (S)-(6-amino-1-hydroxyhexan-2-yl)carbamate
85535-54-2

tert-butyl (S)-(6-amino-1-hydroxyhexan-2-yl)carbamate

Conditions
ConditionsYield
With ammonia; sodiumA 14.7%
B 22%
C 20 % Chromat.
With ammonia; sodium Product distribution;A 14.7%
B 22%
C 20 % Chromat.
tert-butyl (S)-(1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl)carbamate
83351-75-1

tert-butyl (S)-(1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl)carbamate

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

3-(4-hydroxyphenyl)propanoic acid amide
23838-70-2

3-(4-hydroxyphenyl)propanoic acid amide

C

N-(tert-butyloxycarbonyl)-L-tyrosinol
83345-46-4

N-(tert-butyloxycarbonyl)-L-tyrosinol

Conditions
ConditionsYield
With sodium; ammonium chloride In ammoniaA 8%
B 12%
C n/a
N-(tert-butyloxycarbonyl) azide
1070-19-5

N-(tert-butyloxycarbonyl) azide

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With ammonia; water
With diiron nonacarbonyl In benzene
tert-butyl chloroformate
24608-52-4

tert-butyl chloroformate

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With ammonia
nitrobiuret
16326-62-8

nitrobiuret

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With water
tert-butyl cyanoformate
57022-34-1

tert-butyl cyanoformate

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With ammonium hydroxide
3-Brom-propionylcarbamidsaeure-tert.-butylester
99768-94-2

3-Brom-propionylcarbamidsaeure-tert.-butylester

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With sodium hydroxide
tert-butylhypochlorite
507-40-4

tert-butylhypochlorite

Cyclohexyl isocyanate
3173-53-3

Cyclohexyl isocyanate

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
In Petroleum ether
tert-butylhypochlorite
507-40-4

tert-butylhypochlorite

phenyl-diazenecarboxylic acid amide
4203-28-5

phenyl-diazenecarboxylic acid amide

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
In chloroform
sodium cyanide
143-33-9

sodium cyanide

tert-butyl alcohol
75-65-0

tert-butyl alcohol

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With trifluoroacetic acid In benzene
(S)-2-[(tert-butoxycarbonyl)amino]-3-phenylpropionamide
88463-18-7

(S)-2-[(tert-butoxycarbonyl)amino]-3-phenylpropionamide

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

3-phenylpropionamide
102-93-2

3-phenylpropionamide

C

(S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol
66605-57-0

(S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With sodium; ammonium chloride In ammonia
N-(1-aminoisobityl)carbamic acid tert-butyl ester hydrochloride
78497-71-9

N-(1-aminoisobityl)carbamic acid tert-butyl ester hydrochloride

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

ammonia
7664-41-7

ammonia

C

isobutyraldehyde
78-84-2

isobutyraldehyde

Conditions
ConditionsYield
With phosphoric acid at 40 - 45℃; Product distribution; Rate constant; Mechanism; influence of pH;
tert-butyl (S)-(1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl)carbamate
83351-75-1

tert-butyl (S)-(1-amino-3-(4-hydroxyphenyl)-1-oxopropan-2-yl)carbamate

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

3-phenylpropionamide
102-93-2

3-phenylpropionamide

C

(S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol
66605-57-0

(S)-N-tert-butoxycarbonyl-2-amino-3-phenylpropanol

Conditions
ConditionsYield
With sodium; ammonium chloride In ammonia
Nα,Nca-di-tert-butyloxycarbonylasparagine
98115-12-9

Nα,Nca-di-tert-butyloxycarbonylasparagine

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

Boc-Asp-OH
13726-67-5

Boc-Asp-OH

Conditions
ConditionsYield
With sodium hydroxide
Nα,Nca-di-tert-butyloxycarbonylglutamine
98115-14-1

Nα,Nca-di-tert-butyloxycarbonylglutamine

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

Boc-Glu
2419-94-5

Boc-Glu

Conditions
ConditionsYield
With sodium hydroxide
hydroxy sulfonylurea
5663-07-0

hydroxy sulfonylurea

tert-butyl alcohol
75-65-0

tert-butyl alcohol

A

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

ammonium salt of/the/ tert-butylsulfuric acid

ammonium salt of/the/ tert-butylsulfuric acid

Conditions
ConditionsYield
With diethyl ether
N-<(tert-butoxycarbonyl)amino>methylamine hydrochloride
73017-98-8

N-<(tert-butoxycarbonyl)amino>methylamine hydrochloride

A

formaldehyd
50-00-0

formaldehyd

B

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

C

NH3

NH3

Conditions
ConditionsYield
With water-d2 Rate constant;
di-tert-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

4-amino-benzoic acid
150-13-0

4-amino-benzoic acid

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
With sodium hydroxide In tetrahydrofuran; methanol; water28.11 g (68%)
N-t-butyloxycarbonyl-Nε-benzyloxycarbonyl-lysine pentafluorophenyl ester
50903-59-8

N-t-butyloxycarbonyl-Nε-benzyloxycarbonyl-lysine pentafluorophenyl ester

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
Multi-step reaction with 3 steps
1: 90.5 percent / 25percent NH4OH / dioxane / 1 h
2: 94 percent / 1) 10percent Pd/C, H2 / methanol / Ambient temperature; 1) 1 h
3: 14.7 percent / Na, liq. NH3
View Scheme
Nε-(benzyloxycarbonyl)-Nα-(tert-butoxycarbonyl)-L-lysinamide
55592-81-9

Nε-(benzyloxycarbonyl)-Nα-(tert-butoxycarbonyl)-L-lysinamide

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: 94 percent / 1) 10percent Pd/C, H2 / methanol / Ambient temperature; 1) 1 h
2: 14.7 percent / Na, liq. NH3
View Scheme
oxalamic Acid Tert-butyl Ester
35454-04-7

oxalamic Acid Tert-butyl Ester

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Conditions
ConditionsYield
Multi-step reaction with 2 steps
1: (CF3CO)2O / pyridine
2: aq. NH3
View Scheme
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

tert-butyl N,N-dichlorocarbamate
54957-94-7

tert-butyl N,N-dichlorocarbamate

Conditions
ConditionsYield
With hydrogenchloride; calcium hypochlorite In dichloromethane; water at 0 - 1℃; for 0.916667h;100%
With sodium hypochlorite; acetic acid at 0 - 5℃; for 0.266667h;86%
With hydrogenchloride; calcium hypochlorite In dichloromethane; water at 0℃; for 1.75h; regiospecific reaction;84%
With hydrogenchloride; calcium hypochlorite In dichloromethane
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Glyoxilic acid
298-12-4

Glyoxilic acid

Nα-(tert-butoxycarbonyl)-α-hydroxyglycine
96625-24-0

Nα-(tert-butoxycarbonyl)-α-hydroxyglycine

Conditions
ConditionsYield
In acetone for 4h; Heating;100%
In diethyl ether for 72h; Ambient temperature;2.5 g
In diethyl ether for 72h; Ambient temperature;
In acetone for 5h; Heating;
In acetone Heating;
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

sodium benzenesulfonate
873-55-2

sodium benzenesulfonate

benzaldehyde
100-52-7

benzaldehyde

tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate
155396-71-7

tert-butyl N-(phenyl(phenylsulfonyl)methyl)carbamate

Conditions
ConditionsYield
With formic acid In methanol; water at 20℃; for 72h;100%
In methanol; formic acid; water at 20℃; for 72h;99%
In methanol; formic acid; water at 20℃; for 72h;98%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

tert-butyl N,N-dibromocarbamate
358365-86-3

tert-butyl N,N-dibromocarbamate

Conditions
ConditionsYield
With bromine; sodium hydroxide In water at 20℃; for 2h;100%
With bromine; potassium carbonate In water at 20℃; for 2h;
4-benzyloxy-3-formyl-benzonitrile
446026-44-4

4-benzyloxy-3-formyl-benzonitrile

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

4-benzyloxy-3-tert-butoxycarbonylaminomethylbenzonitrile
758710-64-4

4-benzyloxy-3-tert-butoxycarbonylaminomethylbenzonitrile

Conditions
ConditionsYield
With triethylsilane; trifluoroacetic acid In acetonitrile at 20℃; for 2h;100%
C17H24BrNO3Si

C17H24BrNO3Si

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

A-cis

A-cis

Conditions
ConditionsYield
With caesium carbonate; 4,5-bis-(di-tert-butyl-phosphanyl)-9,9-dimethyl-9H-xanthene; palladium diacetate In 1,4-dioxane at 110℃; for 16h;100%
2-benzyl-1,2,3,3a,8,8a-hexahydro-2,7a-diaza-cyclopenta[a]inden-7-one

2-benzyl-1,2,3,3a,8,8a-hexahydro-2,7a-diaza-cyclopenta[a]inden-7-one

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

7-oxo-3a,7,8,8a-tetrahydro-1H,3H-2,7a-diaza-cyclopenta[a]indene-2-carboxylic acid tert-butyl ester
891772-49-9

7-oxo-3a,7,8,8a-tetrahydro-1H,3H-2,7a-diaza-cyclopenta[a]indene-2-carboxylic acid tert-butyl ester

Conditions
ConditionsYield
With hydrogen; palladium(II) hydroxide/carbon In methanol at 50℃; under 2327.23 Torr; for 3h;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

3-[6'-chloro-4'-(3,4-dimethyl-2-oxo-2,3-dihydro-benzoxazole-6-carbonyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl]-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one
1146732-04-8

3-[6'-chloro-4'-(3,4-dimethyl-2-oxo-2,3-dihydro-benzoxazole-6-carbonyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-4-yl]-7-methoxy-1,3,4,5-tetrahydro-benzo[d][1,3]diazepin-2-one

tert-butyl [4'-(3,4-dimethyl-2-oxo-2,3-dihydro-benzoxazole-6-carbonyl)-4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-6'-yl]-carbamate
1146733-74-5

tert-butyl [4'-(3,4-dimethyl-2-oxo-2,3-dihydro-benzoxazole-6-carbonyl)-4-(7-methoxy-2-oxo-1,2,4,5-tetrahydro-benzo[d][1,3]diazepin-3-yl)-3,4,5,6-tetrahydro-2H-[1,2']bipyridinyl-6'-yl]-carbamate

Conditions
ConditionsYield
With caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; tris-(dibenzylideneacetone)dipalladium(0) In 1,4-dioxane for 15h; Reflux;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

4-(4-bromothiazolo[5,4-c]pyridin-2-yl)-3-chloro-5-fluorobenzonitrile
1365992-18-2

4-(4-bromothiazolo[5,4-c]pyridin-2-yl)-3-chloro-5-fluorobenzonitrile

[2-(2-chloro-4-cyano-6-fluorophenyl)thiazolo[5,4-c]pyridin-4-yl]-carbamic acid tert-butyl ester
1365992-31-9

[2-(2-chloro-4-cyano-6-fluorophenyl)thiazolo[5,4-c]pyridin-4-yl]-carbamic acid tert-butyl ester

Conditions
ConditionsYield
With potassium phosphate; tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In water; toluene at 60℃; for 4h; Inert atmosphere;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

4-(7-bromo-[1,2,4]triazolo[1,5-a]pyridine-2-yl)morpholine
1380331-16-7

4-(7-bromo-[1,2,4]triazolo[1,5-a]pyridine-2-yl)morpholine

tert-butyl 2-morpholino-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamate
1380331-17-8

tert-butyl 2-morpholino-[1,2,4]triazolo[1,5-a]pyridin-7-ylcarbamate

Conditions
ConditionsYield
With caesium carbonate; tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In 1,4-dioxane at 110℃; for 20h; Inert atmosphere; Sealed tube;100%
With caesium carbonate; tris-(dibenzylideneacetone)dipalladium(0); 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In 1,4-dioxane at 110℃; for 20h; Inert atmosphere;
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

5-((5-bromopyridin-3-yl)oxy)pyrimidine
1279461-93-6

5-((5-bromopyridin-3-yl)oxy)pyrimidine

tert-butyl (5-(pyrimidin-5-yloxy)pyridin-3-yl)carbamate
1279461-97-0

tert-butyl (5-(pyrimidin-5-yloxy)pyridin-3-yl)carbamate

Conditions
ConditionsYield
With sodium t-butanolate; tert-butyl XPhos; tris(dibenzylideneacetone)dipalladium(0) chloroform complex In toluene at 20℃;100%
2,2,5-trimethyl-4-oxo-4H-1,3-benzodioxin-7-yl trifluoromethanesulfonate
940289-71-4

2,2,5-trimethyl-4-oxo-4H-1,3-benzodioxin-7-yl trifluoromethanesulfonate

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

C16H21NO5

C16H21NO5

Conditions
ConditionsYield
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In 1,4-dioxane at 80℃; for 5h; Inert atmosphere;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

methyl 2-{N-[(1RS)-cyclohex-2-en-1-yl]acetamido}acetate

methyl 2-{N-[(1RS)-cyclohex-2-en-1-yl]acetamido}acetate

tert-butyl (2-{N-acetyl-N-[(1RS)-cyclohex-2-en-1-yl]amino}acetyl)carbamate

tert-butyl (2-{N-acetyl-N-[(1RS)-cyclohex-2-en-1-yl]amino}acetyl)carbamate

Conditions
ConditionsYield
With lithium tert-butoxide In tetrahydrofuran at -23 - 20℃; for 48h; Inert atmosphere;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

methyl 2-{N-[(1RS)-cyclohex-2-en-1-yl]-N-(methoxycarbonyl)amino}acetate

methyl 2-{N-[(1RS)-cyclohex-2-en-1-yl]-N-(methoxycarbonyl)amino}acetate

tert-butyl N-(2-{N-(methoxycarbonyl)-N-[(1RS)-cyclohex-2-en-1-yl]amino}acetyl)carbamate

tert-butyl N-(2-{N-(methoxycarbonyl)-N-[(1RS)-cyclohex-2-en-1-yl]amino}acetyl)carbamate

Conditions
ConditionsYield
With lithium tert-butoxide In tetrahydrofuran at -23 - 20℃; for 48h; Inert atmosphere;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

2-chloro-4-methyl-6-(trifluoromethyl)pyridine

2-chloro-4-methyl-6-(trifluoromethyl)pyridine

tert-butyl (4-methyl-6-(trifluoromethyl)pyridin-2-yl)carbamate

tert-butyl (4-methyl-6-(trifluoromethyl)pyridin-2-yl)carbamate

Conditions
ConditionsYield
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; XPhos In 1,4-dioxane at 80℃; for 2h; Inert atmosphere;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

acetic acid 3-bromo-5-tert-butylbenzyl ester

acetic acid 3-bromo-5-tert-butylbenzyl ester

acetic acid 3-tert-butoxycarbonylamino-5-tert-butylbenzyl ester

acetic acid 3-tert-butoxycarbonylamino-5-tert-butylbenzyl ester

Conditions
ConditionsYield
With palladium diacetate; caesium carbonate; XPhos In 1,4-dioxane at 95℃; for 18h;100%
ethyl 5-bromo-2-methyl-pyridine-3-carboxylate

ethyl 5-bromo-2-methyl-pyridine-3-carboxylate

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

ethyl 5-((tert-butoxycarbonyl)amino)-2-methylnicotinate
301666-75-1

ethyl 5-((tert-butoxycarbonyl)amino)-2-methylnicotinate

Conditions
ConditionsYield
With tris-(dibenzylideneacetone)dipalladium(0); caesium carbonate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene In 1,4-dioxane at 85℃; for 18h; Inert atmosphere;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

N-carbobenzyloxy-L-tryptophane
7432-21-5

N-carbobenzyloxy-L-tryptophane

tert-butyl 2-(((benzyloxy)carbonyl)-L-tryptophyl)hydrazine-1-carboxylate

tert-butyl 2-(((benzyloxy)carbonyl)-L-tryptophyl)hydrazine-1-carboxylate

Conditions
ConditionsYield
With triethylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate In dichloromethane at 20℃; for 3h;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

(S)-N-(1-(3-bromophenyl)ethyl)-3-chloro-2-methylbenzenesulfonamide

(S)-N-(1-(3-bromophenyl)ethyl)-3-chloro-2-methylbenzenesulfonamide

(S)-tert-butyl (3-(1-(3-chloro-2-methylphenylsulfonamido)ethyl)phenyl)carbamate

(S)-tert-butyl (3-(1-(3-chloro-2-methylphenylsulfonamido)ethyl)phenyl)carbamate

Conditions
ConditionsYield
With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; tert-butyl XPhos In toluene for 16h; Sealed tube;100%
(S)-2-methyl-1-[(2-nitrophenyl)sulfonyl]aziridine

(S)-2-methyl-1-[(2-nitrophenyl)sulfonyl]aziridine

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

tert-butyl (S)-{2-[(2-nitrophenyl)sulfonamido]propyl}carbamate

tert-butyl (S)-{2-[(2-nitrophenyl)sulfonamido]propyl}carbamate

Conditions
ConditionsYield
Stage #1: tert-butyl carbazate With potassium hexamethylsilazane In tetrahydrofuran at -78℃; for 0.5h; Inert atmosphere;
Stage #2: (S)-2-methyl-1-[(2-nitrophenyl)sulfonyl]aziridine In tetrahydrofuran; dichloromethane at 20℃; for 18h; Inert atmosphere;
100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

ethyl 6-chloro-3-(3-((6-fluoro-3-((4-methoxybenzyl)thio)naphthalen-1-yl)oxy)propyl)-7-(2-formyl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-1-methyl-1H-indole-2-carboxylate

ethyl 6-chloro-3-(3-((6-fluoro-3-((4-methoxybenzyl)thio)naphthalen-1-yl)oxy)propyl)-7-(2-formyl-5,6-dihydro-4H-pyrrolo[1,2-b]pyrazol-3-yl)-1-methyl-1H-indole-2-carboxylate

ethyl 7-(2-(((tert-butoxycarbonyl)amino)methyl)-5,6-dihydro-4H- pyrrolo[1,2-b]pyrazol-3-yl)-6-chloro-3-(3-((6-fluoro-3-((4-methoxybenzyl)thio)naphthalen-1-yl)oxy)propyl)-1-methyl-1H-indole-2-carboxylate

ethyl 7-(2-(((tert-butoxycarbonyl)amino)methyl)-5,6-dihydro-4H- pyrrolo[1,2-b]pyrazol-3-yl)-6-chloro-3-(3-((6-fluoro-3-((4-methoxybenzyl)thio)naphthalen-1-yl)oxy)propyl)-1-methyl-1H-indole-2-carboxylate

Conditions
ConditionsYield
With triethylsilane; trifluoroacetic acid In dichloromethane at 0 - 20℃; Inert atmosphere;100%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

methyl 3-chloropyridazine-5-carboxylate

methyl 3-chloropyridazine-5-carboxylate

methyl 6-(tert-butoxycarbonylamino)pyridazine-4-carboxylate

methyl 6-(tert-butoxycarbonylamino)pyridazine-4-carboxylate

Conditions
ConditionsYield
With tris-(dibenzylideneacetone)dipalladium(0); 1,1'-bis(di-tertbutylphosphino)ferrocene; potassium carbonate In toluene at 75℃; for 6h; Inert atmosphere;100%
2-methallyltrimethylsilane
18292-38-1

2-methallyltrimethylsilane

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

tert-butyl 5-(dimethoxymethyl)-1H-indole-1-carboxylate
913388-24-6

tert-butyl 5-(dimethoxymethyl)-1H-indole-1-carboxylate

(+)-(R)-N-Boc-3-methyl-1-(N-Boc-5-indolyl)but-3-en-1-amine

(+)-(R)-N-Boc-3-methyl-1-(N-Boc-5-indolyl)but-3-en-1-amine

Conditions
ConditionsYield
With triethylsilyl trifluoromethyl sulfonate; C35H31F6N3OS In diethyl ether at -78 - -50℃; for 6h; Catalytic behavior; Reagent/catalyst; Inert atmosphere; Sealed tube; enantioselective reaction;100%
6,11-dihydrodibenzo[b,e]thiepin-11-ol
1745-46-6

6,11-dihydrodibenzo[b,e]thiepin-11-ol

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

(5,11-Dihydro-10-thia-dibenzo[a,d]cyclohepten-5-yl)-carbamic acid tert-butyl ester
51065-32-8

(5,11-Dihydro-10-thia-dibenzo[a,d]cyclohepten-5-yl)-carbamic acid tert-butyl ester

Conditions
ConditionsYield
With toluene-4-sulfonic acid In acetic acid 1) 37 deg C, 6h; 2) room temp., overnight;99%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

(1S,2S)-1-Phenyl-2-((E)-3-phenylselanyl-propenyl)-cyclopropanecarboxylic acid diethylamide

(1S,2S)-1-Phenyl-2-((E)-3-phenylselanyl-propenyl)-cyclopropanecarboxylic acid diethylamide

[1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

[1-((1R,2S)-2-Diethylcarbamoyl-2-phenyl-cyclopropyl)-allyl]-carbamic acid tert-butyl ester

Conditions
ConditionsYield
With N-chloro-succinimide; isopropylamine In methanol for 2h; Ambient temperature;99%
1-bromo-4-methoxy-benzene
104-92-7

1-bromo-4-methoxy-benzene

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

tert-butyl N-(4-methoxyphenyl)carbamate
18437-68-8

tert-butyl N-(4-methoxyphenyl)carbamate

Conditions
ConditionsYield
With di-tert-butyl(2,2-diphenyl-1-methyl-1-cyclopropyl)phosphine; bis(η3-allyl-μ-chloropalladium(II)); sodium t-butanolate In water at 50℃; for 24h; Inert atmosphere; Green chemistry;99%
With di-tert-butyl{2′-isopropoxy-[1,1′-binaphthalen]-2-yl}phosphane; caesium carbonate; bis(dibenzylideneacetone)-palladium(0) In tert-butyl alcohol at 100℃; for 20h; Inert atmosphere;98%
With tris(dibenzylideneacetone)dipalladium(0) chloroform complex; sodium t-butanolate; tert-butyl XPhos In toluene at 17 - 22℃; for 30h; Inert atmosphere;76%
1,2-Epoxyhexane
1436-34-6

1,2-Epoxyhexane

tert-butyl carbamate
4248-19-5

tert-butyl carbamate

B

((S)-2-hydroxyhexyl)carbamic acid tert-butyl ester

((S)-2-hydroxyhexyl)carbamic acid tert-butyl ester

Conditions
ConditionsYield
With air; 4-nitro-benzoic acid; (R,R)-((t-Bu)4-salen)Co(II) In various solvent(s) at 20℃; for 24h;A n/a
B 99%
With (1R,2R)-(-)-N,N'-bis(3,5-di-tert-butylsalicydene)-1,2-cyclohexanediaminocobalt(II); 3-butyl-1-methyl-1H-imidazol-3-ium hexafluorophosphate; 4-nitro-benzoic acid at 20℃; for 10h; optical yield given as %ee; enantioselective reaction;
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

A

(R)-1,2-epoxy-7-octene
105205-70-7

(R)-1,2-epoxy-7-octene

B

((S)-2-hydroxyoct-7-enyl)carbamic acid tert-butyl ester

((S)-2-hydroxyoct-7-enyl)carbamic acid tert-butyl ester

Conditions
ConditionsYield
With air; 4-nitro-benzoic acid; (R,R)-((t-Bu)4-salen)Co(II) In various solvent(s) at 20℃; for 24h;A n/a
B 99%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

Phenyl glycidyl ether
122-60-1

Phenyl glycidyl ether

A

(2R)-1,2-epoxy-3-phenoxypropane
71031-03-3

(2R)-1,2-epoxy-3-phenoxypropane

B

((S)-2-hydroxy-3-phenoxypropyl)carbamic acid tert-butyl ester

((S)-2-hydroxy-3-phenoxypropyl)carbamic acid tert-butyl ester

Conditions
ConditionsYield
With air; 4-nitro-benzoic acid; [(S,S)-N,N’-bis(3,5-di-tertbutylsalicylidene)-1,2-cyclohexanediaminato(2-)]cobalt(II) In various solvent(s) at 20℃; for 24h;A n/a
B 99%
tert-butyl carbamate
4248-19-5

tert-butyl carbamate

4-bromo-1-methyl-1H-pyrrole-2-carboxylic acid methyl ester
1196-90-3

4-bromo-1-methyl-1H-pyrrole-2-carboxylic acid methyl ester

methyl 4-<<(tert-butyloxy)carbonyl>amino>-1-methyl-pyrrole-2-carboxylate
126092-96-4

methyl 4-<<(tert-butyloxy)carbonyl>amino>-1-methyl-pyrrole-2-carboxylate

Conditions
ConditionsYield
With potassium phosphate; N,N`-dimethylethylenediamine; copper(l) iodide In 1,4-dioxane at 110℃; for 48h;99%

4248-19-5Relevant articles and documents

Skeletally Tunable Seven-Membered-Ring Fused Pyrroles

Andreou, Dimitrios,Essien, Nsikak B.,Pubill-Ulldemolins, Cristina,Terzidis, Michael A.,Papadopoulos, Athanasios N.,Kostakis, George E.,Lykakis, Ioannis N.

supporting information, p. 6685 - 6690 (2021/09/11)

We describe a copper-mediated method that enables the synthesis of seven-membered-ring fused pyrroles (7-mrFPs). The protocol proceeds via an in situ spiro-intermediate ring expansion and tolerates a library of 7-mrFP derivatives with a broad range of functional groups in a simple step with tangible parameters and substrate adaptations. These rare 7-mrFPs are now accessible on a millimolar scale, and selected examples exhibit high antioxidant activity.

Stepwise dual targeting and dual responsive polymer micelles for mitochondrion therapy

Wang, Yi,Wei, Guoqing,Yang, Guang,Zhang, Xiaobin,Zhao, Jingya,Zhou, Shaobing

, p. 157 - 169 (2020/03/26)

Methods to selectively destroy mitochondria of tumor cells and induce cell apoptosis with nanomedicine constitute challenges in cancer therapy. In the present study, we develop cell membrane/mitochondria dual targeting and pH/redox dual responsive nanoparticles for mitochondrion therapy. The nanoparticles are fabricated by the self-assembly of triphenylphosphonium (TPP) grafted poly(ethylene glycol)(PEG)-poly(d,L-lactide)(PLA) copolymers (TPP-PEG-ss-PLA) using disulfide bonds as the intermediate linkers. To shield the surface positive charge of the nanoparticles from TPP composition, chondroitin sulfate (CS) is employed to coat the nanoparticles, and this prolongs blood circulation while endowing an active targeting ability to the cell membrane. In acidic lyso-somes/endosomes, the negatively charged CS layer falls away to expose the TPP component. Subsequently, in the cyto-plasm, the nanoparticles can anchor to the mitochondrial outer membrane by TPP-mediated targeting, thereby inducing a decrease in the membrane potential and opening of the permeability transition pore. Thus, the overproduction of ROS in the mitochondria promotes cell apoptosis. The released DOX directly diffuse into the mitochondria, thereby resulting in mito-chondrial DNA damage. Therefore, the nanoparticles exhibit significant potential in terms of a new avenue for mitochondrion therapy in cancer treatment.

An Fe3O4@SiO2/Schiff base/Cu(ii) complex as an efficient recyclable magnetic nanocatalyst for selective mono: N-arylation of primary O-alkyl thiocarbamates and primary O-alkyl carbamates with aryl halides and arylboronic acids

Sardarian, Ali Reza,Dindarloo Inaloo, Iman,Zangiabadi, Milad

, p. 8557 - 8565 (2019/06/14)

An efficient, convenient and novel method for the selective mono N-arylation of primary O-alkyl thiocarbamates and primary O-alkyl carbamates with aryl halides and arylboronic acids in the presence of a recyclable magnetic Cu(ii) nanocatalyst is described. A variety of mono N-arylated O-alkyl thiocarbamates and O-alkyl carbamates were prepared in good to excellent yields with a broad range of aryl coupling partners. The magnetic nanocatalyst can be easily recovered with an external magnetic field and reused at least five times without noticeable leaching or loss of its catalytic activity. This cost-effective and eco-friendly methodology has some other advantages, such as easy preparation of the catalyst, simple workup procedure, and easy purification, which makes this protocol interesting for the users in various fields of pharmacology and biotechnology systems.

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