HCID 21069821, compound → HCID 21069990, compound
Reaction equation
[CH2:1]([O:8][C:9]1[C:18](=[O:19])[N:17]2[C:12]([C:13]([CH3:21])([CH3:20])[O:14][CH2:15][CH2:16]2)=[N:11][C:10]=1[C:22]([OH:24])=O)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:25][CH2:26][C:27]1[CH:38]=[CH:37][C:36]([F:39])=[CH:35][C:28]=1[C:29]([NH:31][CH:32]1[CH2:34][CH2:33]1)=[O:30]>>[CH:32]1([NH:31][C:29]([C:28]2[CH:35]=[C:36]([F:39])[CH:37]=[CH:38][C:27]=2[CH2:26][NH:25][C:22]([C:10]2[N:11]=[C:12]3[N:17]([C:18](=[O:19])[C:9]=2[O:8][CH2:1][C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=2)[CH2:16][CH2:15][O:14][C:13]3([CH3:20])[CH3:21])=[O:24])=[O:30])[CH2:33][CH2:34]1Participants
3
Procedure
The title compound can be prepared from intermediate 27, 3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido-[2,1-c][1,4]oxazine-2-carboxylic acid and intermediate 40, 2-(aminomethyl)-N-cyclopropyl-5-fluorobenzamide. LC/MS m/z 521 (M+H).
Sources & evidence
- ORD record
- ord-28e195532c7c423cbe190ccdd1f39fae
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07157447B2
Reaction notes
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