4-Chlorobenzaldehyde → HCID 10450880, compound

HRID 962639Notes

Reaction equation

[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[C:16]3[CH2:15][CH2:14][NH:13][CH2:12][C:11]=3[C:10](=[O:17])[O:9][C:7]=2[CH:8]=1.[Cl:18][C:19]1[CH:26]=[CH:25][C:22]([CH:23]=O)=[CH:21][CH:20]=1>>[Cl:18][C:19]1[CH:26]=[CH:25][C:22]([CH2:23][N:13]2[CH2:14][CH2:15][C:16]3[C:6]4[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][C:7]=4[O:9][C:10](=[O:17])[C:11]=3[CH2:12]2)=[CH:21][CH:20]=1

Participants

Reactant 2

HCID 77264-Chlorobenzaldehyde

HCID 131369188-Methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one

Product 1

HCID 10450880HCID 10450880, compoundYield 70%

Procedure

Prepared by the procedure of Example 3 from 8-methoxy-1,2,3,4-tetrahydro-chromeno[3,4-c]pyridin-5-one and 4-chlorobenzaldehyde. Yield 70%; mp 140°-142° C.

Sources & evidence

ORD record: ord-3958b0f149fd4d4c80496c3d0ec6881e
Source dataset: uspto-grants-1998_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05760050

Reaction notes

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