2-(2-Amino-thiazol-4-yl)-benzoic acid → benzofuran-4-carboxylic acid {(1S,3S,5S)-2-[2-(2-amino-thiazol-4-yl)-benzoyl]-2-aza-bicyclo[3.1.0]hex-3-ylmethyl}-amide

HRID 2064822Notes

Reaction equation

HRID 2064822 reaction equation
[C@H:1]12[CH2:6][C@H:5]1[CH2:4][C@@H:3]([CH2:7][NH:8][C:9]([C:11]1[CH:12]=[CH:13][CH:14]=[C:15]3[O:19][CH:18]=[CH:17][C:16]=13)=[O:10])[NH:2]2.[NH2:20][C:21]1[S:22][CH:23]=[C:24]([C:26]2[CH:34]=[CH:33][CH:32]=[CH:31][C:27]=2[C:28](O)=[O:29])[N:25]=1>>[NH2:20][C:21]1[S:22][CH:23]=[C:24]([C:26]2[CH:34]=[CH:33][CH:32]=[CH:31][C:27]=2[C:28]([N:2]2[C@H:3]([CH2:7][NH:8][C:9]([C:11]3[CH:12]=[CH:13][CH:14]=[C:15]4[O:19][CH:18]=[CH:17][C:16]=34)=[O:10])[CH2:4][C@H:5]3[C@@H:1]2[CH2:6]3)=[O:29])[N:25]=1

Participants

3

Procedure

prepared by reaction of benzofuran-4-carboxylic acid [(1S,3S,5S)-2-aza-bicyclo[3.1.0]hex-3-ylmethyl]-amide with 2-(2-amino-thiazol-4-yl)-benzoic acid. LC-MS (basic): tR=1.28 min; [M+H]+=458.9.

Sources & evidence

ORD record
ord-17906f6d7584463a9bc18e9170464dfc
Source dataset
uspto-grants-2012_10
Patent number
US08288435B2

Reaction notes

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