Butyl isocyanate → HCID 19431475, compound
Reaction equation
[NH2:1][CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:11]3[CH2:12][CH2:13][C:14](=[O:17])[NH:15][N:16]=3)[CH:8]=2)[CH2:3]1.[CH2:18]([N:22]=[C:23]=[O:24])[CH2:19][CH2:20][CH3:21]>>[CH2:18]([NH:22][C:23]([NH:1][CH:2]1[CH2:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:11]3[CH2:12][CH2:13][C:14](=[O:17])[NH:15][N:16]=3)[CH:8]=2)[CH2:3]1)=[O:24])[CH2:19][CH2:20][CH3:21]Participants
3
Procedure
2-Amino-5-[4,5-dihydropyridazin-3(2H)-on-6-yl]indane and butyl isocyanate were treated in the same manner as in Example 29 to obtain 2-(butylcarbamoyl) amino-5-[4,5-dihydropyridazin-3(2H)-on-6-yl]indane.
Sources & evidence
- ORD record
- ord-6bd340b60116467a8e9995276b0b12c5
- Source dataset
- uspto-grants-1997_02
- Patent number
- US05605901
Reaction notes
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