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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949776Generated: November 1, 2026

Tetrahydrofuran → (4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-2-yl)(3,4-dihydroquinolin-1(2H)-yl)methanone

https://huagongshe.com/reaction/1949776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantTriethylamineHCID 8471—
Reactant1,2,3,4-TetrahydroquinolineHCID 69460—
Reactant4,5-Dihydrobenzo[b]thieno[2,3-d]oxepine-2-carbonylchlorideHCID 57900147—
Product(4,5-dihydrobenzo[b]thieno[2,3-d]oxepin-2-yl)(3,4-dihydroquinolin-1(2H)-yl)methanoneHCID 57900106—

Reaction Steps

To a solution of 1,2,3,4-tetrahydroquinoline (0.755 mmol) and triethylamine (0.105 mL, 0.755 mmol) in tetrahydrofuran (1.5 mL, 18 mmol) was added 4,5-dihydrobenzo[b]thieno[2,3-d]oxepine-2-carbonylchloride (0.100 g, 0.378 mmol) portionwise as a solid. Reaction was stirred at room temperature with monitor for formation of desired product. The reaction was stirred overnight. After aqueous workup, the crude was taken into DMF at a concentrated of 100 mg/ml and purified by preparative RP-HPLC to give 218 (yield 80% of theoretical). MS: (ESI+) 362.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399690B2
Source datasetuspto-grants-2013_03
ORD IDord-0b7c66e0a9024c659307be0b6716a707
Source noteuspto-grants-2013_03