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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1504326Generated: November 2, 2026

Hydrochloric Acid → HCID 89541653, compound

https://huagongshe.com/reaction/1504326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTetrahydrofuranHCID 8028—
ReactantTrimethyl borateHCID 8470—
ReactantHCID 89541530HCID 89541530—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 89541653HCID 8954165357%

Reaction Conditions

Temperature0 °C

Reaction Steps

Under an atmosphere of nitrogen, a mixture of N-(4-bromo-2-chloro-5-trifluoromethoxy-phenyl)-6-[(R)-4-(2,2-dimethyl-propionyl)-2-methyl-piperazin-1-yl]-nicotinamide (20.0 g, 34.6 mmol) and tetrahydrofuran (200 mL) was cooled to 0° C. and then 1.3 M isopropylmagnesium chloride lithium chloride complex in tetrahydrofuran (79.9 mL, 104 mmol) was added dropwise at 0-10° C. After 2.5 h, boric acid, trimethyl ester (12.0 mL, 106 mmol) was added dropwise, and then 1 N HCl (105 mL) was added and the reaction mixture was stirred overnight. The reaction mixture was extracted with EtOAc (250 mL); the organic layer was washed with water, sat. aq. NaHCO3, dried over MgSO4, and evaporated to give crude product (22.8 g). To the crude product was added ethanol (230 mL) and then slowly water (57.5 mL). The resulting mixture was stirred for 10 days and filtered to give the title intermediate as a crystalline solid (10.7 g, 57% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09212168B2
Source datasetuspto-grants-2015_12
ORD IDord-4cda94daa19547999a3a16d50a9151d1
Source noteuspto-grants-2015_12