3,5-Dimethylisoxazole-4-isocyanate → HCID 44187238, compound
Reaction equation
C(O[C:4]([C:6]1[CH:7]=[N:8][C:9]2[C:14]([C:15]=1[NH:16][CH:17]1[CH2:21][CH2:20][CH2:19][CH2:18]1)=[CH:13][CH:12]=[CH:11][C:10]=2[O:22][CH3:23])=[O:5])C.[N:24]([C:27]1[C:28]([CH3:33])=[N:29][O:30][C:31]=1[CH3:32])=[C:25]=[O:26]>>[CH:17]1([N:16]2[C:15]3[C:14]4[CH:13]=[CH:12][CH:11]=[C:10]([O:22][CH3:23])[C:9]=4[N:8]=[CH:7][C:6]=3[C:4](=[O:5])[N:24]([C:27]3[C:28]([CH3:33])=[N:29][O:30][C:31]=3[CH3:32])[C:25]2=[O:26])[CH2:21][CH2:20][CH2:19][CH2:18]1Participants
3
Procedure
1-Cyclopentyl-3-(3,5-dimethyl-isoxazol-4-yl)-7-methoxy-1H-pyrimido[5,4-c]quinoline-2,4-dione (17 mg) was prepared from 4-cyclopentylamino-8-methoxy-quinoline-3-carboxylic acid ethyl ester (0.1 mmol) and 4-isocyanato-3,5-dimethyl-isoxazole (0.05 mmol) following general procedure C. LCMS: m/z 407 [M+1]+.
Sources & evidence
- ORD record
- ord-0be7bb7784e94d0aa2e6fe439e567717
- Source dataset
- uspto-grants-2011_06
- Patent number
- US07964608B2
Reaction notes
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