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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449384Generated: October 25, 2026

(1-Isopropylpiperidin-4-yl)methanamine → 2-Chloropropane

https://huagongshe.com/reaction/1449384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1-Isopropylpiperidin-4-yl)methanamineHCID 7258859—
Reactant3-Chloro-6-chlorocarbonylphenylsulfenyl chlorideHCID 10728826—
Product2-ChloropropaneHCID 6361—
ProductN-(piperidin-4-ylmethyl)acetamideHCID 4341747—

Reaction Steps

2-(1-isopropylpiperid-4-ylmethyl)-6-chloro-1,2-benzisothiazolin-3-one is obtained analogously to Example 33 by reacting 3-chloro-6-chlorocarbonylphenylsulfenyl chloride and 1-isopropyl-4-aminomethylpiperidine [boiling point 15: 95°-97° C.; obtained from 4-acetylaminomethylpiperidine and isopropyl chloride analogously to Singh et al., J. Med. Chem. 12, 949 (1969) and Werbel et al., supra]. After recrystallization in acetone, yellow crystals of melting point 134°-135° C. are obtained; yield: 37% of theory.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04190663
Source datasetuspto-grants-1980_02
ORD IDord-aeae6fcd82d04f3aaad0ba67c05d7052
Source noteuspto-grants-1980_02