N-(tert-butyloxycarbonyl)-S-(triphenylmethyl)-L-cysteinylglycine methyl ester

Base Information

Chemical Name:N-(tert-butyloxycarbonyl)-S-(triphenylmethyl)-L-cysteinylglycine methyl ester
CAS No.:52071-18-8
Molecular Formula:C₃₀H₃₄N₂O₅S
Molecular Weight:534.676
Hs Code.:

Synonyms:N-(tert-butyloxycarbonyl)-S-(triphenylmethyl)-L-cysteinylglycine methyl ester

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

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Chemical Property of N-(tert-butyloxycarbonyl)-S-(triphenylmethyl)-L-cysteinylglycine methyl ester

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Technology Process of N-(tert-butyloxycarbonyl)-S-(triphenylmethyl)-L-cysteinylglycine methyl ester

There total 2 articles about N-(tert-butyloxycarbonyl)-S-(triphenylmethyl)-L-cysteinylglycine methyl 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: 98.0%

: 21947-98-8,87494-13-1
N-tert-butyloxycarbonyl-S-trityl-L-cysteine

: 616-34-2
methoxycarbonylmethylamine

: 52071-18-8
N-(tert-butyloxycarbonyl)-S-(triphenylmethyl)-L-cysteinylglycine methyl ester

Guidance literature:: With benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 2h; pH=8;
DOI:10.1002/ejoc.200700698

Reference yield: 83.0%

: 21947-98-8,87494-13-1
N-tert-butyloxycarbonyl-S-trityl-L-cysteine

: 5680-79-5,883886-67-7
glycine ethyl ester hydrochloride

: 52071-18-8
N-(tert-butyloxycarbonyl)-S-(triphenylmethyl)-L-cysteinylglycine methyl ester

Guidance literature:: With sodium hydrogencarbonate; benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at 20 ℃; for 4h; Inert atmosphere;
DOI:10.1021/ja9088549