2-methylpropyl (2S)-2-aminopropanoate → N-[(2-phenylthiothienyl)acetyl]alanine iso-butyl ester

HRID 1953608Notes

Reaction equation

HRID 1953608 reaction equation
[C:1]1([S:7][C:8]2[S:9][CH:10]=[CH:11][C:12]=2[CH2:13][C:14]([OH:16])=O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:17]([O:21][C:22](=[O:26])[C@H:23]([CH3:25])[NH2:24])[CH:18]([CH3:20])[CH3:19]>>[CH2:17]([O:21][C:22](=[O:26])[C@H:23]([CH3:25])[NH:24][C:14](=[O:16])[CH2:13][C:12]1[CH:11]=[CH:10][S:9][C:8]=1[S:7][C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)[CH:18]([CH3:20])[CH3:19]

Participants

3

Reactant 2

HCID 137435562-methylpropyl (2S)-2-aminopropanoateHCID 54517004(2-Phenylthiothienyl)acetic acid

Product 1

HCID 53734580N-[(2-phenylthiothienyl)acetyl]alanine iso-butyl ester

Procedure

Following General Procedure I above, and using (2-phenylthiothienyl)acetic acid and alanine iso-butyl ester (prepared following General Procedure J above), the title compound was prepared. The reaction was monitored by tlc on silica gel and purification was by filtration as described in the general procedure.

Workup

  1. customThe reaction was monitored by tlc on silica gel and purification
  2. filtrationwas by filtration

Sources & evidence

ORD record
ord-fd91a875f6204d3681839ff23c5579a8
Source dataset
uspto-grants-2000_09
Patent number
US06117901

Reaction notes

Loading…