3-(Chloromethyl)benzoyl chloride → HCID 12043166, compound

HRID 2187105Notes

Reaction equation

HRID 2187105 reaction equation
[CH2:1]([C@H:8]1[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][S:16]([C:19]2[CH:24]=[CH:23][C:22]([OH:25])=[CH:21][CH:20]=2)(=[O:18])=[O:17])[CH2:10][C@H:9]1[OH:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:27][CH2:28][C:29]1[CH:30]=[C:31]([CH:35]=[CH:36][CH:37]=1)[C:32](Cl)=[O:33]>>[CH2:1]([C@H:8]1[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][S:16]([C:19]2[CH:24]=[CH:23][C:22]([O:25][C:32](=[O:33])[C:31]3[CH:35]=[CH:36][CH:37]=[C:29]([CH2:28][Cl:27])[CH:30]=3)=[CH:21][CH:20]=2)(=[O:18])=[O:17])[CH2:10][C@H:9]1[OH:26])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

Participants

3

Reactant 2

HCID 27333243-(Chloromethyl)benzoyl chlorideHCID 9885963(3S,4S)-4-[2-(4-benzyl-3-hydroxy-piperidin-1-yl)-ethanesulfonyl]-phenol

Product 1

HCID 12043166HCID 12043166, compoundYield 80%

Procedure

The title compound was prepared from (3S,4S)-4-[2-(4-benzyl-3-hydroxy-piperidin-1-yl)-ethanesulfonyl]-phenol and 3-chlormethylbenzoylchloride in 80% yield as a colorless solid.

Sources & evidence

ORD record
ord-1c99d6f515a14cc195ae1c77d5f68085
Source dataset
uspto-grants-2002_06
Patent number
US06407235B1

Reaction notes

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