Dicyclohexylamine → 3-[2-(3,3-Dicyclohexyl-ureido)-thiazole-5-sulfonylamino]-propionic acid
Reaction equation
[CH:1]1([N:7]([CH:24]2[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]2)[C:8](=[O:23])[NH:9][C:10]2[S:11][C:12]([S:15]([NH:18]CC(O)=O)(=[O:17])=[O:16])=[CH:13][N:14]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.C1(NC2CCCCC2)CCCCC1.C([O:45][C:46](=[O:59])[CH2:47][CH2:48]NS(C1SC(N)=NC=1)(=O)=O)C>>[CH:1]1([N:7]([CH:24]2[CH2:25][CH2:26][CH2:27][CH2:28][CH2:29]2)[C:8](=[O:23])[NH:9][C:10]2[S:11][C:12]([S:15]([NH:18][CH2:48][CH2:47][C:46]([OH:59])=[O:45])(=[O:17])=[O:16])=[CH:13][N:14]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
4
Procedure
Prepared in a similar manner to [2-(3,3-dicyclohexyl-ureido)-thiazole-5-sulfonylamino]-acetic acid via dicyclohexylamine and 3-(2-amino-thiazole-5-sulfonylamino)-propionic acid ethyl ester to give the title compound.
Sources & evidence
- ORD record
- ord-07e27589b1224bc2ac399395e1160455
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07582769B2
Reaction notes
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