Pyridine → 4-Hydroxymethyl-piperidine-1-carboxylic acid (7-methoxy-4-morpholin-4-yl-thiazolo[5,4-c]pyridin-2-yl)-amide
Reaction equation
C1(O[C:8](=[O:27])[NH:9][C:10]2[S:11][C:12]3[C:13]([N:21]4[CH2:26][CH2:25][O:24][CH2:23][CH2:22]4)=[N:14][CH:15]=[C:16]([O:19][CH3:20])[C:17]=3[N:18]=2)C=CC=CC=1.[OH:28][CH2:29][CH:30]1[CH2:35][CH2:34][NH:33][CH2:32][CH2:31]1.N1C=CC=CC=1>ClC(Cl)C.O1CCCC1>[CH3:20][O:19][C:16]1[C:17]2[N:18]=[C:10]([NH:9][C:8]([N:33]3[CH2:34][CH2:35][CH:30]([CH2:29][OH:28])[CH2:31][CH2:32]3)=[O:27])[S:11][C:12]=2[C:13]([N:21]2[CH2:22][CH2:23][O:24][CH2:25][CH2:26]2)=[N:14][CH:15]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
From (7-methoxy-4-morpholin-4-yl-thiazolo[5,4-c]pyridin-2-yl)-carbamic acid phenyl ester with 4-(hydroxymethyl)piperidine and pyridine in dichloroethane and tetrahydrofuran. ES-MS m/e (%): 408 (M+H+, 100).
Sources & evidence
- ORD record
- ord-07d6eeea94f142ba885acea8504786c4
- Source dataset
- uspto-grants-2007_09
- Patent number
- US07273865B2
Reaction notes
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