Pyrrolidine → 2-{2-[(2-Chloro-6-fluoro-phenyl)-pyrrolidin-1-yl-methyl]-pyrrol-1-yl}-phenylamine

HRID 1796934Notes

Reaction equation

HRID 1796934 reaction equation
[N:1]1([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[NH2:12])[CH:5]=[CH:4][CH:3]=[CH:2]1.[Cl-].[Cl:14][C:15]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[C:16]=1[CH:17]=[N+:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1.ClC1C=CC=C(F)C=1C=O.N1CCCC1>>[Cl:14][C:15]1[CH:26]=[CH:25][CH:24]=[C:23]([F:27])[C:16]=1[CH:17]([N:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1)[C:5]1[N:1]([C:6]2[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=2[NH2:12])[CH:2]=[CH:3][CH:4]=1

Participants

5

Reactant 4

HCID 31268PyrrolidineHCID 678472-Chloro-6-fluorobenzaldehydeHCID 801232-(1H-pyrrol-1-yl)anilineHCID 179122731-(2-Chloro-6-fluoro-benzylidene)-pyrrolidinium chloride

Product 1

HCID 99475312-{2-[(2-Chloro-6-fluoro-phenyl)-pyrrolidin-1-yl-methyl]-pyrrol-1-yl}-phenylamine

Procedure

The preparation was carried out in accordance with general synthesis instructions 4 from 2-pyrrol-1-yl-phenylamine and 1-(2-chloro-6-fluoro-benzylidene)-pyrrolidinium chloride, which had been prepared in accordance with example 4 from 2-chloro-6-fluorobenzaldehyde and pyrrolidine.

Sources & evidence

ORD record
ord-d4777731201a44b8b7d3595257622a11
Source dataset
uspto-grants-2006_04
Patent number
US07034018B2

Reaction notes

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