2-Furancarbonyl chloride → HCID 18317977, compound
Reaction equation
Cl.[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12]1[CH:11]([C:17]3([C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH2:20][CH2:19][CH2:18]3)[NH:10][CH2:9][CH2:8][C:7]2=1.[O:26]1[CH:30]=[CH:29][CH:28]=[C:27]1[C:31](Cl)=[O:32]>>[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12]1[CH:11]([C:17]3([C:21]([O:23][CH2:24][CH3:25])=[O:22])[CH2:20][CH2:19][CH2:18]3)[N:10]([C:31]([C:27]3[O:26][CH:30]=[CH:29][CH:28]=3)=[O:32])[CH2:9][CH2:8][C:7]2=1Participants
3
Procedure
The procedure is as in Example 55, using as substrate the compound of Example 7 and as reagent 2-furoyl chloride.
Sources & evidence
- ORD record
- ord-d2025e0123ee434f8cd5f90cdb67300f
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06350757B1
Reaction notes
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