8-Boc-3,8-diaza-bicyclo(3.2.1)octane → 3-(5-Chloro-7-morpholin-4-yl-thiazolo[5,4-d]pyrimidin-2-ylmethyl)-3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester
Reaction equation
C(OC(N1CC2C([CH2:11][N:12]([CH2:16][C:17]3[S:18][C:19]4[N:20]=[C:21]([Cl:32])[N:22]=[C:23]([N:26]5[CH2:31][CH2:30][O:29][CH2:28][CH2:27]5)[C:24]=4[N:25]=3)[CH2:13]2)C1)=O)(C)(C)C.[C:33]([O:37][C:38]([N:40]1[CH:45]2[CH2:46][CH2:47][CH:41]1CNC2)=[O:39])([CH3:36])([CH3:35])[CH3:34]>>[C:33]([O:37][C:38]([N:40]1[CH:45]2[CH2:46][CH2:47][CH:41]1[CH2:11][N:12]([CH2:16][C:17]1[S:18][C:19]3[N:20]=[C:21]([Cl:32])[N:22]=[C:23]([N:26]4[CH2:27][CH2:28][O:29][CH2:30][CH2:31]4)[C:24]=3[N:25]=1)[CH2:13]2)=[O:39])([CH3:36])([CH3:34])[CH3:35]Participants
3
Reactant 2
Product 1
Procedure
Prepared according to the method used in the preparation of 5-(5-chloro-7-morpholin-4-yl-thiazolo[5,4-d]pyrimidin-2-ylmethyl)-hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl ester using 3,8-diaza-bicyclo[3.2.1]octane-8-carboxylic acid tert-butyl ester in place of hexahydro-pyrrolo[3,4-c]pyrrole-2-carboxylic acid tert-butyl ester. The title compound was obtained as a white solid (91 mg, 95%).
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-c7e8493ec6d84f4f98c30c610506cc52
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07893060B2
Reaction notes
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