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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 540108Generated: October 25, 2026

2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine 1,1-dioxide → 4-(4-Chloro-6-(trifluoromethoxy)quinolin-2-yl)-2,3,4,5-tetrahydro-1,4-benzothiazepine 1,1-dioxide

https://huagongshe.com/reaction/540108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine 1,1-dioxideHCID 19608196—
Reactant2,4-Dichloro-6-(trifluoromethoxy)quinolineHCID 82581137—
Solvent1-ButanolHCID 263—
Product4-(4-Chloro-6-(trifluoromethoxy)quinolin-2-yl)-2,3,4,5-tetrahydro-1,4-benzothiazepine 1,1-dioxideHCID 7125456977%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 2,4-dichloro-6-(trifluoromethoxy)quinoline (250 mg, 0.89 mmol), 2,3,4,5-tetrahydro-1,4-benzothiazepine 1,1-dioxide (210 mg, 1.06 mmol) and n-butanol (2 mL) was heated with stirring in a 5 mL of microwave process vial for 3 hours at 150° C. under microwave irradiation. The mixture was filtered. The formed solid was collected by filtration and washed with 10 mL of mixture solution of petroleum ether and ethyl acetate (V/V=10/1) to afford 0.3 g of the product (yield was 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871756B2
Source datasetuspto-grants-2014_10
ORD IDord-f869f477935f45f6a007826bc4f6b8fb
Source noteuspto-grants-2014_10