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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842049Generated: October 30, 2026

Benzoyl chloride → HCID 56942374, compound

https://huagongshe.com/reaction/1842049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantHCID 66613260HCID 66613260—
SolventDichloromethaneHCID 6344—
ProductHCID 56942374HCID 56942374—

Reaction Conditions

Temperature0 °C

Reaction Steps

In a flask, dichloromethane (0.023mL) was added to benzoyl chloride. The reaction was cooled to 0° C., and a solution of N-(3-(pyridin-4-yl)-1H-indazol-5-yl)piperidine-3-carboxamide (0.014 g, 0.044 mmol) in dichloromethane (0.020 mL) was dropwise added to the benzoyl chloride solution. The reaction stirred for 6 hrs from 0° C. to room temperature. The reaction was quenched with water (1 mL) and extracted with dichloromethane (3×1 mL). The extracts were combined and dried with sodium sulfate. The crude product was purified using prep LC/MS. LC-MS: 426.1 [M+H]. LC/MS RT=2.998 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946216B2
Source datasetuspto-grants-2015_02
ORD IDord-322925a831ae4e199b1f8442506e456b
Source noteuspto-grants-2015_02