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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748126Generated: November 1, 2026

Ethanesulfonylchloride, 2-chloro- → HCID 66748921, compound

https://huagongshe.com/reaction/1748126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
ReactantSodium hydrideHCID 24758—
ReactantHCID 66748666HCID 66748666—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66748921HCID 66748921—

Reaction Steps

To a suspension of NaH (60%, 35.5 mg) in THF (dry) (5 mL) was added 2-chloroethanesulfonyl chloride (0.056 mL) at 0° C. and the mixture was stirred for 5 min at the same temperature. A solution of 3-(3′-methoxybiphenyl-4-yl)pyridin-2-amine (49 mg) in THF (dry) (5 mL) was added at 0° C. and the mixture was stirred at room temperature overnight. The mixture was quenched with water. Water and EtOAc were added and the extracted organic layer was washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was washed with EtOAc and dried in vacuo to give the title compound (18 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150591B2
Source datasetuspto-grants-2015_10
ORD IDord-69a46f8d1c1347889b4cf4ccf7152ff5
Source noteuspto-grants-2015_10