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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846763Generated: November 1, 2026

2-Chlorobenzothiazole → N-(3-(3-chloropyrazin-2-yloxy)cyclobutyl)benzo[d]thiazol-2-amine

https://huagongshe.com/reaction/1846763

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChlorobenzothiazoleHCID 11987—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-(3-Chloro-pyrazin-2-yloxy)-cyclobutylamine hydrochlorideHCID 86660160—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductN-(3-(3-chloropyrazin-2-yloxy)cyclobutyl)benzo[d]thiazol-2-amineHCID 5854852295.5%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 3-(3-chloro-pyrazin-2-yloxy)-cyclobutylamine hydrochloride (1.2 g, 6.28 mmol), 2-chloro-benzothiazole (purchased from ALDRICH™) (1.07 g, 6.28 mmol) and DIEA (1.8 g, 12.56 mmol) in NMP (12 mL) was heated to 180° C. for 2 hours in microwave. The reaction mixture was extracted with EtOAc (40 mL) and water, the organic phase was washed with brine and dried over Na2SO4. The organic layers were concentrated and purified by column chromatography on silica gel to give N-(3-((3-chloropyrazin-2-yl)oxy)cyclobutyl)benzo[d]thiazol-2-amine (3.0 g, 6 mmol, 95.5%). ESI-MS (M+1): 333 calc. for C15H13ClN4OS 332.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952037B2
Source datasetuspto-grants-2015_02
ORD IDord-b37da26e7ec1446abda4dc122919990c
Source noteuspto-grants-2015_02