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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120168Generated: October 31, 2026

6-Chloro-2-benzothiazolamine → HCID 12093897, compound

https://huagongshe.com/reaction/2120168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-2-benzothiazolamineHCID 7226—
ReactantThionyl ChlorideHCID 24386—
ReactantAmmonium 2-[[1-(4-pyridinyl)piperidin-4-ylmethyl]amino]pyridine-3-carboxylateHCID 11174879—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 12093897HCID 1209389711.1%

Reaction Steps

A solution of ammonium 2-[[1-(4-pyridinyl)piperidin-4-ylmethyl]amino]pyridine-3-carboxylate (400 mg, 1.28 mmol) in methylene chloride (5 mL) was treated with thionyl chloride (0.112 mL, 1.54 mmol) and the mixture was heated at reflux. After 3 h, the mixture was cooled and then treated dropwise with a solution of 2-amino-6-chlorobenzothiazole (284 mg, 1.54 mmol) in pyridine (5 mL). After 1 h, the mixture was concentrated in the presence of silica gel. The residue was purified by column chromatography (SiO2: 1 to 4% [2 N ammonia in methanol]:chloroform) followed by recrystallization from methanol to yield 68 mg (11%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689780B1
Source datasetuspto-grants-2004_02
ORD IDord-6a7e3735d29a4c47bb1dbd91ec3431ee
Source noteuspto-grants-2004_02