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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,3,4,5-Tetrahydrobenzo[F][1,4]thiazepine 1,1-dioxide | HCID 19608196 | — |
| Reactant | 2,4-Dichloro-6-(trifluoromethoxy)quinoline | HCID 82581137 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 4-(4-Chloro-6-(trifluoromethoxy)quinolin-2-yl)-2,3,4,5-tetrahydro-1,4-benzothiazepine 1,1-dioxide | HCID 71254569 | 77% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871756B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f869f477935f45f6a007826bc4f6b8fb |
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| Source note | uspto-grants-2014_10 |
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