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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424449Generated: November 1, 2026

Chlorotrimethylsilane → HCID 178497302, compound

https://huagongshe.com/reaction/1424449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantHCID 66611125HCID 66611125—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 178497302HCID 17849730290.2%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of methyl 4-carbamoyl-3-(2,2-difluoro-2-(4-fluorophenyl)acetamido)benzoate (1.3 g, 3.5 mmol) in DCE (20 mL) were added triethylamine (20 mL, 142 mmol) and trimethylsilyl chloride (6.7 mL, 53.2 mmol and the mixture was heated 85° C. overnight. The mixture was allowed to cool to rt, and then was concentrated under reduced pressure. The residue was partitioned between EtOAc (150 mL) and H2O (100 mL), and the separated aqueous phase was extracted with EtOAc (3×150 mL). The combined organic layers were washed with brine (100 mL), dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was treated with MeOH with sonication, and the solid was collected by filtration to afford methyl 2-(difluoro(4-fluorophenyl)methyl)-4-hydroxyquinazoline-7-carboxylate (1.1 g, 89%). 1H NMR (300 MHz, DMSO-d6) δ 3.91 (s, 3H), 7.39 (t, 2H), 7.78 (t, 2H), 8.06 (d, 1H), 8.16 (s, 1H), 8.27 (d, 1H), 13.34 (s, 1H); LC-MS (ESI) m/z 349 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927711B2
Source datasetuspto-grants-2015_01
ORD IDord-9a06dfd908c24098b1b12611a26a010c
Source noteuspto-grants-2015_01