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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2405959Generated: October 31, 2026

Ethyl chloroformate → HCID 44518473, compound

https://huagongshe.com/reaction/2405959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl chloroformateHCID 10928—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 16665563HCID 16665563—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 44518473HCID 4451847386%

Reaction Steps

To a solution of N-[5-(3,5-difluoro-benzenesulfonyl)-4,5,6,7-tetrahydro-1H-pyrazolo[4,3-c]pyridin-3-yl]-4-(4-methyl-piperazin-1-yl)-2-(tetrahydro-pyran-4-ylamino)-benzamide (1.38 g, 2.24 mmol) in anhydrous THF (150 mL), cooled to −40° C., under argon, was added lithium bis(trimethylsilyl)amide 1.0 M in THF (2.35 mL, 2.35 mmol). The mixture was stirred for 5 min. then ethyl chloroformate (0.225 mL, 2.35 mmol) was added. The reaction was stirred at −40° C. for 1 h, then was poured in water and extracted with ethyl acetate. The organic phase was washed with water, brine and dried with sodium sulfate. After filtration and evaporation the crude was triturated with ether to give the title compound as white solid (1.32 g, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809337B2
Source datasetuspto-grants-2014_08
ORD IDord-589f9bfa43824a90983935574dfb20dd
Source noteuspto-grants-2014_08