Glycine methyl ester hydrochloride → HCID 57883539, compound
Reaction equation
[CH:1]1([N:7]([CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)[C:8](=[O:18])[NH:9][C:10]2[S:11][C:12]([C:15](O)=[O:16])=[CH:13][N:14]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.Cl.[CH3:26][O:27][C:28](=[O:31])[CH2:29][NH2:30]>>[CH3:26][O:27][C:28](=[O:31])[CH2:29][NH:30][C:15]([C:12]1[S:11][C:10]([NH:9][C:8]([N:7]([CH:19]2[CH2:24][CH2:23][CH2:22][CH2:21][CH2:20]2)[CH:1]2[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]2)=[O:18])=[N:14][CH:13]=1)=[O:16]Participants
3
Procedure
Prepared in 75% yield as described in general procedure (K) using 2-(3,3-dicyclohexylureido)-thiazole-5-carboxylic acid and glycine methyl ester hydrochloride.
Workup
- customPrepared in 75% yield
Sources & evidence
- ORD record
- ord-84951703bf5b4a359e166b0f22ebabd6
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08263634B2
Reaction notes
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