[4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester

Base Information

Chemical Name:[4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester
CAS No.:1027276-16-9
Molecular Formula:C₂₅H₂₇N₅O₃
Molecular Weight:445.521
Hs Code.:

Synonyms:[4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester

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Chemical Property of [4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester

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Technology Process of [4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester

There total 8 articles about [4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 84.0%

: 185399-96-6
N-(t-butoxycarbonyl)-4-tributylstannylaniline

: 135795-50-5
5,11-dihydro-11-ethyl-5-methyl-2-<<(trifluoromethyl)-sulfonyl>oxy>-6H-dipyrido<3,2-b:2',3'-e><1,4>diazepin-6-one

: 1027276-16-9
[4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester

Guidance literature:: With bis-triphenylphosphine-palladium(II) chloride; lithium chloride; In N,N-dimethyl-formamide; at 115 ℃; for 4h;
DOI:10.1021/jm00024a010

Reference yield:

: 6628-77-9
6-methoxy-pyridin-3-ylamine

: 1027276-16-9
[4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 8 steps

1: 60 percent / NaOAc, Br₂ / acetic acid / 0.33 h

2: 90 percent / pyridine / CH₂Cl₂ / 0.33 h / Ambient temperature

3: 1.) NaH, DMSO / 1.) 50 deg C, 2.) DMSO, 30 min

4: 76 percent / xylene / 4 h / 150 °C

5: 76 percent / NaH / xylene / 2 h / 150 °C

6: 98 percent / 48percent aq. HBr, AcOH / 0.08 h / Heating

7: 77 percent / diisopropylethylamine / CHCl₃

8: 84 percent / Pd(Ph₃P)2Cl₂, LiCl / dimethylformamide / 4 h / 115 °C

With pyridine; bis-triphenylphosphine-palladium(II) chloride; hydrogen bromide; bromine; sodium acetate; sodium hydride; acetic acid; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; lithium chloride; In dichloromethane; chloroform; acetic acid; N,N-dimethyl-formamide; xylene;
DOI:10.1021/jm00024a010

Reference yield:

: 135795-46-9
2-bromo-6-methoxy-pyridin-3-ylamine

: 1027276-16-9
[4-(5-Ethyl-10-methyl-11-oxo-10,11-dihydro-5H-4,5,6,10-tetraaza-dibenzo[a,d]cyclohepten-7-yl)-phenyl]-carbamic acid tert-butyl ester

Guidance literature:: Multi-step reaction with 7 steps

1: 90 percent / pyridine / CH₂Cl₂ / 0.33 h / Ambient temperature

2: 1.) NaH, DMSO / 1.) 50 deg C, 2.) DMSO, 30 min

3: 76 percent / xylene / 4 h / 150 °C

4: 76 percent / NaH / xylene / 2 h / 150 °C

5: 98 percent / 48percent aq. HBr, AcOH / 0.08 h / Heating

6: 77 percent / diisopropylethylamine / CHCl₃

7: 84 percent / Pd(Ph₃P)2Cl₂, LiCl / dimethylformamide / 4 h / 115 °C

With pyridine; bis-triphenylphosphine-palladium(II) chloride; hydrogen bromide; sodium hydride; acetic acid; dimethyl sulfoxide; N-ethyl-N,N-diisopropylamine; lithium chloride; In dichloromethane; chloroform; N,N-dimethyl-formamide; xylene;
DOI:10.1021/jm00024a010