Aniline → HCID 14502083, compound

HRID 1723088Notes

Reaction equation

HRID 1723088 reaction equation
CO[C:3]1[CH:8]=[CH:7][C:6]([N:9]2[C:21]3[C:20]4[CH:19]=[CH:18][CH:17]=[N:16][C:15]=4[N:14]([C:22]4[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=4)[C:13](=[O:28])[C:12]=3[CH2:11][CH2:10]2)=[CH:5][CH:4]=1.COC1C=CC(N)=CC=1.NC1C=CC=CC=1>>[C:6]1([N:9]2[C:21]3[C:20]4[CH:19]=[CH:18][CH:17]=[N:16][C:15]=4[N:14]([C:22]4[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=4)[C:13](=[O:28])[C:12]=3[CH2:11][CH2:10]2)[CH:5]=[CH:4][CH:3]=[CH:8][CH:7]=1

Participants

4

Reactant 3

HCID 6115AnilineHCID 7732P-Anisidine2×HCID 20067591HCID 20067591, compound

Product 1

HCID 14502083HCID 14502083, compound

Procedure

This procedure will also produce 1,2,3,5-tetrahydro-1-(4-methoxyphenyl)-5-phenyl-4H-pyrrolo [3,2-c][1,8]naphthyridin-4-one when 4-methoxyaniline (also known as p-anisidine) is substituted for aniline.

Sources & evidence

ORD record
ord-7a9532c80dde4f54ac04af0a3fdaf52a
Source dataset
uspto-grants-1989_08
Patent number
US04859669

Reaction notes

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