4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

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Chemical Name:4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester
CAS No.:646532-28-7
Molecular Formula:C₄₁H₅₆N₆O₁₂
Molecular Weight:824.929
Hs Code.:

4-benzyloxycarbonylamino-4-(1-{<i>N</i>'-<i>tert</i>-butoxycarbonylmethyl-<i>N</i>'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid <i>tert</i>-butyl ester

Synonyms:4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

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Chemical Property of 4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

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Technology Process of 4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

There total 6 articles about 4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric 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: 32.0%

: 646533-03-1
(2R,3R)-3-(1-carbamoyl-2-phenylethylcarbamoyl)oxirane-2-carboxylic acid

: 646532-80-1
Cbz-Glu(O-t-Bu)-Val-NHNHCH₂COO-t-Bu

: 646532-28-7
4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: (2R,3R)-3-(1-carbamoyl-2-phenylethylcarbamoyl)oxirane-2-carboxylic acid; With 4-methyl-morpholine; isobutyl chloroformate; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h;

Cbz-Glu(O-t-Bu)-Val-NHNHCH₂COO-t-Bu; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/jm0305016

Reference yield:

: 5292-43-3
bromoacetic acid tert-butyl ester

: 646532-28-7
4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 2 steps

1.1: 78 percent / 4-methylmorpholine / dimethylformamide / 20.5 h / -10 - 20 °C

2.1: N-methylmorpholine; isobutyl chloroformate / dimethylformamide / 0.5 h / 0 °C

2.2: 32 percent / dimethylformamide / 0 - 20 °C

With 4-methyl-morpholine; isobutyl chloroformate; In N,N-dimethyl-formamide;
DOI:10.1021/jm0305016

Reference yield:

: 5241-58-7
L-Phenylalanine amide

: 646532-28-7
4-benzyloxycarbonylamino-4-(1-{N'-tert-butoxycarbonylmethyl-N'-[3-(1-carbamoyl-2-phenyl-ethylcarbamoyl)-oxiranecarbonyl]-hydrazinocarbonyl}-2-methyl-propylcarbamoyl)-butyric acid tert-butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: 1-hydroxybenzotriazole; 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride / CHCl₃ / 17 h / 0 - 20 °C

2.1: KOH / ethanol

3.1: N-methylmorpholine; isobutyl chloroformate / dimethylformamide / 0.5 h / 0 °C

3.2: 32 percent / dimethylformamide / 0 - 20 °C

With 4-methyl-morpholine; potassium hydroxide; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; isobutyl chloroformate; In ethanol; chloroform; N,N-dimethyl-formamide;
DOI:10.1021/jm0305016