Cyclopropanecarbonyl chloride → HCID 15523513, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:11][CH2:10][CH:9]([C:12]3[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:21])([F:20])[F:19])[CH:13]=3)[N:8]([CH2:22][C:23]#[N:24])[C:7]=2[CH:25]=1.[CH:26]1([C:29](Cl)=[O:30])[CH2:28][CH2:27]1>>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[O:11][CH2:10][CH:9]([C:12]3[CH:17]=[CH:16][CH:15]=[C:14]([C:18]([F:20])([F:21])[F:19])[CH:13]=3)[N:8]([CH2:22][CH2:23][NH:24][C:29]([CH:26]3[CH2:28][CH2:27]3)=[O:30])[C:7]=2[CH:25]=1Participants
3
Procedure
The procedure is as in Example 15, starting from the compound obtained in Step A and with the replacement of benzoyl chloride with cyclopropylcarbonyl chloride.
Sources & evidence
- ORD record
- ord-0d58ef934e5b425d8e7913af2ecece19
- Source dataset
- uspto-grants-2003_09
- Patent number
- US06620809B2
Reaction notes
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