N-Methylbutylamine → N-butyl-5-chloro-N-methyl-pentanesulfonamide

HRID 565737Notes

Reaction equation

HRID 565737 reaction equation
[CH3:1][NH:2][CH2:3][CH2:4][CH2:5][CH3:6].[Cl:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][S:13](Cl)(=[O:15])=[O:14]>>[CH2:3]([N:2]([CH3:1])[S:13]([CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][Cl:7])(=[O:15])=[O:14])[CH2:4][CH2:5][CH3:6]

Participants

3

Reactant 2

HCID 8068N-MethylbutylamineHCID 12589202HCID 12589202, compound

Product 1

HCID 19711033N-butyl-5-chloro-N-methyl-pentanesulfonamideYield 92.8%

Procedure

The reaction was carried out in the same manner as in Preparation Example 11 except for using N-methyl-n-butylamine (5.75g, 66 mmol) in place of diethylamine, and 5-chloropentanesulfonyl chloride (6.15g, 30 mmol) in place of 6-chlorohexanesulfonyl chloride in Preparation Example 11, to give N-n-butyl-N-methyl-5-chloropentanesulfonamide (7.12 g) as a pale yellow oil.

Workup

  1. customThe reaction was carried out in the same manner as in Preparation Example 11 except
  2. customin Preparation Example 11

Sources & evidence

ORD record
ord-4feb31bbe46c41c39782bcc569bca7c1
Source dataset
uspto-grants-2001_01
Patent number
US06172228B2

Reaction notes

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