Isoamylamine → HCID 57668315, compound
Reaction equation
[CH:1]1([N:7]([CH2:21][CH2:22][C:23]2[CH:28]=CC=C[CH:24]=2)[C:8](=[O:20])NC2SC(SCC(O)=O)=CN=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C1(=O)CCCCC1.CC(C)CCN.C([O:44][C:45](=[O:56])[C:46]([S:49][C:50]1[S:54][C:53]([NH2:55])=[N:52][CH:51]=1)([CH3:48])[CH3:47])C>>[CH:1]1([N:7]([CH2:21][CH2:22][CH:23]([CH3:28])[CH3:24])[C:8](=[O:20])[NH:55][C:53]2[S:54][C:50]([S:49][C:46]([CH3:47])([CH3:48])[C:45]([OH:44])=[O:56])=[CH:51][N:52]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
5
Procedure
Prepared as described for the synthesis of [2-(3-cyclohexyl-3-phenethyl-ureido)-thiazol-5-ylsulfanyl]-acetic acid, from cyclohexanone, 3-methylbutylamine and 2-(2-amino-thiazol-5-ylsulfanyl)-2-methyl-propionic acid ethyl ester.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-e58e2021412949578001b46a95a9baf7
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07884210B2
Reaction notes
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