4-Thiazoleacetic acid, 2-amino-, ethyl ester → HCID 59513957, compound
Reaction equation
[CH2:1]([N:8]1[CH:12]=[CH:11][CH:10]=[C:9]1[C:13]([OH:15])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH2:16]([O:18][C:19](=[O:27])[CH2:20][C:21]1[N:22]=[C:23]([NH2:26])[S:24][CH:25]=1)[CH3:17]>>[CH2:16]([O:18][C:19](=[O:27])[CH2:20][C:21]1[N:22]=[C:23]([NH:26][C:13]([C:9]2[N:8]([CH2:1][C:2]3[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=3)[CH:12]=[CH:11][CH:10]=2)=[O:15])[S:24][CH:25]=1)[CH3:17]Participants
3
Procedure
(2-{[1-(Benzyl)-1H-pyrrole-2-carbonyl]-amino}-thiazol-4-yl)acetic acid ethyl ester (60 mg) was prepared from 1-benzyl-pyrrole-2-carboxylic acid (50 mg, 0.25 mmol) and 2-aminothiazol-4-yl acetic acid ethyl ester (47 mg, 0.25 mmol) following general procedure F.
Sources & evidence
- ORD record
- ord-a4149ba328484a56850384f8bee95df2
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08148413B2
Reaction notes
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