((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid butyl ester

Base Information

Chemical Name:((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid butyl ester
CAS No.:322407-85-2
Molecular Formula:C₃₁H₄₁N₃O₁₂
Molecular Weight:647.679
Hs Code.:

((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid butyl ester

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Chemical Property of ((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid butyl ester

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Technology Process of ((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid butyl ester

There total 5 articles about ((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid 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: 5.0%

: 75-36-5
acetyl chloride

: 322405-00-5
2-(4-hydroxymethyl-1,3,4,5-tetrahydroxy-2-piperidinyl)-2-[(N-benzyloxycarbonyl)tyrosylamino]acetic acid

: 71-36-3
butan-1-ol

: 322407-85-2
((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid butyl ester

Guidance literature:: DOI:10.7164/antibiotics.53.1282

Reference yield:

: 501-53-1,94274-21-2
benzyl chloroformate

: 322407-85-2
((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / NaHCO₃ / H₂O / 0.67 h

2: NaBH₄ / dimethylformamide; H₂O

3: 5 percent

With sodium tetrahydroborate; sodium hydrogencarbonate; In water; N,N-dimethyl-formamide;
DOI:10.7164/antibiotics.53.1282

Reference yield:

: 2-(2,4,5,8-tetrahydroxy-7-oxa-2-azabicyclo[3.2.1]oct-3-yl)-2-(tyrosylamino)acetic acid

: 322407-85-2
((1S,2S,3S,4S,5S)-4-Acetoxymethyl-1,3,4,5-tetrahydroxy-piperidin-2-yl)-[(S)-2-benzyloxycarbonylamino-3-(4-hydroxy-phenyl)-propionylamino]-acetic acid butyl ester

Guidance literature:: Multi-step reaction with 3 steps

1: 92 percent / NaHCO₃ / H₂O / 0.67 h

2: NaBH₄ / dimethylformamide; H₂O

3: 5 percent

With sodium tetrahydroborate; sodium hydrogencarbonate; In water; N,N-dimethyl-formamide;
DOI:10.7164/antibiotics.53.1282