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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445522Generated: November 1, 2026

Boron Trichloride → HCID 10074312, compound

https://huagongshe.com/reaction/1445522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantHCID 10047296HCID 10047296—
SolventDichloromethaneHCID 6344—
ProductHCID 10074312HCID 10074312127.1%

Reaction Steps

Preparation of compound 30 (a) (2-(4-fluoro-phenyl)-5-hydroxy-6-morpholin-4-yl-benzofuran-3-carboxylic acid methylamide). Boron trichloride (1M solution in xylenes, 5.0 mL, 5.0 mmol) was added to a solution of 2-(4-fluoro-phenyl)-5-isopropoxy-6-morpholin-4-yl-benzofuran-3-carboxylic acid methylamide (0.71 g, 1.7 mmol, which can be prepared according to Example 24, above), dissolved in dichloromethane (30 mL). The reaction mixture was refluxed for 30 minutes, cooled to room temperature, quenched with 1M hydrochloric acid (10 mL) and stirred for 1 hour. The organics were removed by evaporation, and a saturated solution of sodium bicarbonate was added until pH=8-9. The product was extracted with ethyl acetate and purified via column chromatography (dry loading onto silica gel, ethyl acetate/hexanes gradient) to provide 0.53 g (84%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07666863B2
Source datasetuspto-grants-2010_02
ORD IDord-7cc5dc4909894113b250744e100e51ff
Source noteuspto-grants-2010_02