3-Furaldehyde → HCID 69155743, compound

HRID 750198Notes

Reaction equation

HRID 750198 reaction equation
[CH3:1][O:2][C:3]([C:5]1[N:6]([NH2:23])[C:7](=[O:22])[C:8]2[C:13]([C:14]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[CH:12][C:11]([Cl:21])=[CH:10][CH:9]=2)=[O:4].[O:24]1[CH:28]=[CH:27][C:26]([CH:29]=O)=[CH:25]1>>[CH3:1][O:2][C:3]([C:5]1[N:6]([N:23]=[CH:29][C:26]2[CH:27]=[CH:28][O:24][CH:25]=2)[C:7](=[O:22])[C:8]2[C:13]([C:14]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[CH:12][C:11]([Cl:21])=[CH:10][CH:9]=2)=[O:4]

Participants

3

Reactant 2

HCID 103513-FuraldehydeHCID 69156379HCID 69156379, compound

Product 1

HCID 69155743HCID 69155743, compound

Procedure

The present compound was synthesized by a method similar to that in Example 210 and using 2-amino-6-chloro-1-oxo-4-phenyl-1,2-dihydroisoquinoline-3-carboxylic acid methyl ester (210 mg) and furan-3-carbaldehyde. A colorless powder (130 mg).

Workup

  1. customThe present compound was synthesized by a method similar to that in Example 210

Sources & evidence

ORD record
ord-437ade036f15441f8d3247a5f2b842a0
Source dataset
uspto-grants-2008_07
Patent number
US07402595B2

Reaction notes

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