Glycine → HCID 44193978, compound
Reaction equation
C(O[C:6]([C:8]1[N:13]=[C:12]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:11]2[C:20]([CH2:23][N:24]3[C:32]4[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=4)[CH:26]=[CH:25]3)=[N:21][S:22][C:10]=2[C:9]=1[OH:33])=[O:7])CCC.[NH2:34][CH2:35][C:36]([OH:38])=[O:37]>>[OH:33][C:9]1[C:10]2[S:22][N:21]=[C:20]([CH2:23][N:24]3[C:32]4[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=4)[CH:26]=[CH:25]3)[C:11]=2[C:12]([C:14]2[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=2)=[N:13][C:8]=1[C:6]([NH:34][CH2:35][C:36]([OH:38])=[O:37])=[O:7]Participants
3
Procedure
The title compound was synthesized in analogy Example 1 from 7-hydroxy-3-indol-1-ylmethyl-4-phenyl-isothiazolo[4,5-c]pyridine-6-carboxylic acid butyl ester and glycine: MS (m/z) 459.1 (M+1).
Sources & evidence
- ORD record
- ord-fe04858e4dc348d7a6eb402df0d059cf
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08952160B2
Reaction notes
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