N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine methyl ester

Base Information

Chemical Name:N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine methyl ester
CAS No.:78537-16-3
Molecular Formula:C₃₉H₅₇N₅O₁₀
Molecular Weight:755.909
Hs Code.:

Synonyms:N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine methyl ester

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Chemical Property of N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine methyl ester

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Technology Process of N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine methyl ester

There total 4 articles about N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine 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: 60.0%

: 78537-15-2
N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serine

: 76698-53-8
glycyl-L-phenylalanyl-L-leucine methyl ester trifluoroacetate

: 78537-16-3
N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine methyl ester

Guidance literature:: With benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; chloroform; a) 0 deg C, 1 h, b) RT, overnight;
DOI:10.1021/jm00142a002

Reference yield:

: 3978-80-1
Boc-Tyr-OH

: 78537-16-3
N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / triethylamine, 1-hydroxybenzotriazole (HOBT), dicyclohexylcarbodiimide (DCC) / tetrahydrofuran; CHCl₃ / a) 0 deg C, 1 h, b) RT, overnight

2: 94 percent / 1 N NaOH / methanol / a) 0 deg C, 30 min, b) RT, 2 h

3: 60 percent / triethylamine, 1-hydroxybenzotriazole (HOBT), dicyclohexylcarbodiimide (DCC) / tetrahydrofuran; CHCl₃ / a) 0 deg C, 1 h, b) RT, overnight

With sodium hydroxide; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; chloroform;
DOI:10.1021/jm00142a002

Reference yield:

: 78537-14-1
O-tert-butyl-D-serine methyl ester hydrochloride

: 78537-16-3
N-(tert-butyloxycarbonyl)-L-tyrosyl-O-tert-butyl-D-serylglycyl-L-phenylalanyl-L-leucine methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 89 percent / triethylamine, 1-hydroxybenzotriazole (HOBT), dicyclohexylcarbodiimide (DCC) / tetrahydrofuran; CHCl₃ / a) 0 deg C, 1 h, b) RT, overnight

2: 94 percent / 1 N NaOH / methanol / a) 0 deg C, 30 min, b) RT, 2 h

3: 60 percent / triethylamine, 1-hydroxybenzotriazole (HOBT), dicyclohexylcarbodiimide (DCC) / tetrahydrofuran; CHCl₃ / a) 0 deg C, 1 h, b) RT, overnight

With sodium hydroxide; benzotriazol-1-ol; triethylamine; dicyclohexyl-carbodiimide; In tetrahydrofuran; methanol; chloroform;
DOI:10.1021/jm00142a002