4-Chlorobenzaldehyde → HCID 10807035, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[C:15]3[CH2:14][CH2:13][NH:12][CH2:11][C:10]=3[C:9](=[O:16])[O:8][C:6]=2[CH:7]=1.[Cl:17][C:18]1[CH:25]=[CH:24][C:21]([CH:22]=O)=[CH:20][CH:19]=1>>[Cl:17][C:18]1[CH:25]=[CH:24][C:21]([CH2:22][N:12]2[CH2:13][CH2:14][C:15]3[C:5]4[CH:4]=[CH:3][C:2]([CH3:1])=[CH:7][C:6]=4[O:8][C:9](=[O:16])[C:10]=3[CH2:11]2)=[CH:20][CH:19]=1Participants
3
Procedure
Prepared by the procedure of Example 3 from 8-methyl-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one* and 4-chlorobenzaldehyde. Yield 65%; mp 147°-149° C.
Sources & evidence
- ORD record
- ord-7a36fc6232e44eccbc82903fa67278ff
- Source dataset
- uspto-grants-1998_06
- Patent number
- US05760050
Reaction notes
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