C₃₀H₄₀ClN₅O₄

Base Information

Chemical Name:C₃₀H₄₀ClN₅O₄
CAS No.:1396257-79-6
Molecular Formula:C₃₀H₄₀ClN₅O₄
Molecular Weight:570.132
Hs Code.:

C<sub>30</sub>H<sub>40</sub>ClN<sub>5</sub>O<sub>4</sub>

Synonyms:

Suppliers and Price of C₃₀H₄₀ClN₅O₄

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of C₃₀H₄₀ClN₅O₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₀H₄₀ClN₅O₄

There total 12 articles about C₃₀H₄₀ClN₅O₄ 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:

: 1001271-08-4
tert-butyl (S)-3-((R)-4-benzyl-2-oxooxazolidin-3-yl)-2-(4-chlorophenyl)-3-oxopropyl(cyclopropylmethyl)carbamate

: 1396257-79-6
C₃₀H₄₀ClN₅O₄

Guidance literature:: Multi-step reaction with 2 steps

1: lithium hydroxide; water; dihydrogen peroxide / tetrahydrofuran / 12 h / 0 °C

2: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / 4 h / 0 - 20 °C

With water; dihydrogen peroxide; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran;
DOI:10.1021/jm301024w

Reference yield:

: 1001180-47-7
tert-butyl 4-((5R,7R)-5-methyl-7-((4-nitrobenzoyl)oxy)-6,7-dihydro-5H-cyclopenta[d]pyrimidin-4-yl)-piperazine-1-carboxylate

: 1396257-79-6
C₃₀H₄₀ClN₅O₄

Guidance literature:: Multi-step reaction with 3 steps

1: lithium hydroxide; water / tetrahydrofuran / 1 h / 0 °C

2: hydrogenchloride / dichloromethane; 1,4-dioxane / 0 - 20 °C / Inert atmosphere

3: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / 4 h / 0 - 20 °C

With hydrogenchloride; water; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; dichloromethane;
DOI:10.1021/jm301024w

Reference yield:

: 85440-74-0
(2R)-2-methyl-5-oxocyclopentanecarboxylic acid ethyl ester

: 1396257-79-6
C₃₀H₄₀ClN₅O₄

Guidance literature:: Multi-step reaction with 11 steps

1.1: ammonium acetate / methanol

2.1: ammonium formate / 24 h / 150 °C

3.1: trichlorophosphate / 1,2-dichloro-ethane / 6 h / Reflux

4.1: N-ethyl-N,N-diisopropylamine / butan-1-ol / 16 h / Reflux; Inert atmosphere

5.1: sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid / chloroform / 4.67 h / 0 - 20 °C / Inert atmosphere

6.1: 2 h / 100 °C / Inert atmosphere

7.1: lithium hydroxide / tetrahydrofuran / 16 h / 20 °C

8.1: oxalyl dichloride / dichloromethane; dimethyl sulfoxide / 1 h / -78 °C

8.2: 0.5 h / -78 - 20 °C

9.1: triethylamine; formic acid / dichloromethane / 0.25 h / Inert atmosphere

9.2: Inert atmosphere

10.1: hydrogenchloride / dichloromethane; 1,4-dioxane / 0 - 20 °C / Inert atmosphere

11.1: N-ethyl-N,N-diisopropylamine; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate / 4 h / 0 - 20 °C

With hydrogenchloride; formic acid; oxalyl dichloride; ammonium acetate; ammonium formate; sodium hydrogencarbonate; O-(1H-benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate; triethylamine; N-ethyl-N,N-diisopropylamine; 3-chloro-benzenecarboperoxoic acid; lithium hydroxide; trichlorophosphate; In tetrahydrofuran; 1,4-dioxane; methanol; dichloromethane; chloroform; dimethyl sulfoxide; 1,2-dichloro-ethane; butan-1-ol; 8.1: |Swern Oxidation;
DOI:10.1021/jm301024w