Tert-Butylamine → HCID 13242988, compound
Reaction equation
[O:1]1[CH:3]([CH3:4])[CH:2]1[O:5][C:6]1[CH:11]=[CH:10][C:9]([C:12]2[N:21]([CH:22]([CH3:24])[CH3:23])[C:20](=[O:25])[C:19]3[C:14](=[CH:15][CH:16]=[C:17]([O:26][CH3:27])[CH:18]=3)[N:13]=2)=[CH:8][CH:7]=1.[C:28]([NH2:32])([CH3:31])([CH3:30])[CH3:29]>>[OH:1][CH:3]([CH2:4][NH:32][C:28]([CH3:31])([CH3:30])[CH3:29])[CH2:2][O:5][C:6]1[CH:7]=[CH:8][C:9]([C:12]2[N:21]([CH:22]([CH3:23])[CH3:24])[C:20](=[O:25])[C:19]3[C:14](=[CH:15][CH:16]=[C:17]([O:26][CH3:27])[CH:18]=3)[N:13]=2)=[CH:10][CH:11]=1Participants
3
Procedure
This compound was prepared analogous to Example 1 from 2-[4-(1,2-epoxy-propoxy)-phenyl]-3-isopropyl-6-methoxy-3,4-dihydro-quinazolin-4-one and tert. butylamine.
Sources & evidence
- ORD record
- ord-d4fb7d7e9cdc40a386ebac2b9bf30f38
- Source dataset
- uspto-grants-1983_04
- Patent number
- US04379788
Reaction notes
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