(5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide

Base Information

Chemical Name:(5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide
CAS No.:141249-10-7
Molecular Formula:C₂₃H₃₁N₅O₅S₂
Molecular Weight:521.662
Hs Code.:

(5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide

Synonyms:(5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide

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Chemical Property of (5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide

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Technology Process of (5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide

There total 8 articles about (5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide 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:

: 141249-06-1
Ac-Cys(Acm)-Pro-Phe-Cys(Acm)-NHMe

: 141249-10-7
(5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide

Guidance literature:: With iodine; In methanol;
DOI:10.1021/ja00037a003

Reference yield:

: 13734-34-4
N-tert-butoxycarbonyl-L-phenylalanine

: 141249-10-7
(5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide

Guidance literature:: Multi-step reaction with 4 steps

1: dicyclohexylcarbodiimide (DCC), 1-hydroxybenzotriazole (HOBt)

2: HCl / ethyl acetate

3: dicyclohexylcarbodiimide (DCC), 1-hydroxybenzotriazole (HOBt)

4: I₂ / methanol

With hydrogenchloride; iodine; benzotriazol-1-ol; dicyclohexyl-carbodiimide; In methanol; ethyl acetate;
DOI:10.1021/ja00037a003

Reference yield:

: 5497-76-7,184719-80-0,256478-96-3
L-proline tert-butyl ester hydrochloride

: 141249-10-7
(5R,10R,13S,15aS)-5-Acetylamino-13-benzyl-4,12,15-trioxo-dodecahydro-7,8-dithia-3a,11,14-triaza-cyclopentacyclotetradecene-10-carboxylic acid methylamide

Guidance literature:: Multi-step reaction with 4 steps

1: dicyclohexylcarbodiimide (DCC), 1-hydroxybenzotriazole (HOBt)

2: 1.) TFA

3: dicyclohexylcarbodiimide (DCC), 1-hydroxybenzotriazole (HOBt)

4: I₂ / methanol

With iodine; benzotriazol-1-ol; dicyclohexyl-carbodiimide; trifluoroacetic acid; In methanol;
DOI:10.1021/ja00037a003