3,5-Dimethoxybenzoyl chloride → [3-(3,4-Dichlorophenyl)-3-(2-hydroxyethyl)-1-pyrrolidinyl](3,5-dimethoxyphenyl)methanone

HRID 1682981Notes

Reaction equation

HRID 1682981 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([CH2:14][CH2:15][OH:16])[CH2:13][CH2:12][NH:11][CH2:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8].[CH3:17][O:18][C:19]1[CH:20]=[C:21]([CH:25]=[C:26]([O:28][CH3:29])[CH:27]=1)[C:22](Cl)=[O:23]>>[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2([CH2:14][CH2:15][OH:16])[CH2:13][CH2:12][N:11]([C:22](=[O:23])[C:21]3[CH:25]=[C:26]([O:28][CH3:29])[CH:27]=[C:19]([O:18][CH3:17])[CH:20]=3)[CH2:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8]

Participants

3

Reactant 2

HCID 870033,5-Dimethoxybenzoyl chlorideHCID 184644272-(3-(3,4-Dichlorophenyl)pyrrolidin-3-yl)ethanol

Product 1

HCID 54501447[3-(3,4-Dichlorophenyl)-3-(2-hydroxyethyl)-1-pyrrolidinyl](3,5-dimethoxyphenyl)methanone

Procedure

The method of example 3.1 was used with 2-[3-(3,4-dichloro-phenyl)-pyrrolidin-3-yl]-ethanol (1 mmol) and 3,5-dimethoxy-benzoyl chloride (1 mmol) to prepare the title compound. Chromatography on silica gel eluting sequentially with ethyl acetate and then 6% methanol in dichloromethane gave the title compound.

Sources & evidence

ORD record
ord-78aa84ec03754ff99ac79bff446d99e9
Source dataset
uspto-grants-1997_06
Patent number
US05635510

Reaction notes

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