(S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid methyl ester

Base Information

Chemical Name:(S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid methyl ester
CAS No.:872864-31-8
Molecular Formula:C₂₅H₃₀N₄O₄
Molecular Weight:450.538
Hs Code.:

Synonyms:(S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid methyl ester

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Chemical Property of (S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid methyl ester

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Technology Process of (S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid methyl ester

There total 5 articles about (S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid 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: 96.0%

: 7524-50-7
methyl (2S)-2-amino-3-phenylpropanoate hydrochloride

: 143327-79-1
((S)-1-benzyl-2-prop-2-ynyl)carbamic acid t-butyl ester

: 872864-31-8
(S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid methyl ester

Guidance literature:: methyl (2S)-2-amino-3-phenylpropanoate hydrochloride; With triflic azide; copper(II) sulfate; triethylamine; In methanol; dichloromethane; water; at 20 ℃; for 18h;

((S)-1-benzyl-2-prop-2-ynyl)carbamic acid t-butyl ester; With tert-Butyl 2,2,2-trichloroacetimidate; copper(II) sulfate; sodium L-ascorbate; In methanol; dichloromethane; water; at 100 ℃; for 0.0833333h; Further stages.; microwave irradiation;
DOI:10.1021/jo701292h

Reference yield: 76.0%

: 116911-32-1
(S)-2-azido-3-phenylpropionic acid methyl ester

: 143327-79-1
((S)-1-benzyl-2-prop-2-ynyl)carbamic acid t-butyl ester

: 872864-31-8
(S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid methyl ester

Guidance literature:: With copper(II) sulfate; sodium L-ascorbate; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; In tert-butyl alcohol; at 20 ℃; for 16h;
DOI:10.1021/ja056406z

Reference yield:

: 72155-45-4
Boc-L-phenylalaninal

: 872864-31-8
(S)-2-[4-((S)-1-tert-Butoxycarbonylamino-2-phenyl-ethyl)-[1,2,3]triazol-1-yl]-3-phenyl-propionic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 98 percent / PPh₃ / CH₂Cl₂ / -78 °C

2: 75 percent / n-butyllithium / tetrahydrofuran / -78 °C

3: 76 percent / aq. CuSO₄; tris(1-benzyl-1H-[1,2,3]triazol-4-ylmethyl)-amine; sodium L-ascorbate / 2-methyl-propan-2-ol / 16 h / 20 °C

With n-butyllithium; copper(II) sulfate; sodium L-ascorbate; triphenylphosphine; tris[(1-benzyl-1H-1,2,3-triazol-4yl)methyl]amine; In tetrahydrofuran; dichloromethane; tert-butyl alcohol; 1: Corey-Fuchs homologation reaction;
DOI:10.1021/ja056406z