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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166191Generated: November 2, 2026

Benzenesulfonyl chloride → HCID 12085355, compound

https://huagongshe.com/reaction/1166191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
ReactantHCID 12085354HCID 12085354—
SolventTetrahydrofuranHCID 8028—
ProductHCID 12085355HCID 12085355—

Reaction Steps

A stirred solution of tert-butyl 5-[(5-fluoro-1H-indol-3-yl)methyl]-3,6-dihydro-1(2H)-pyridinecarboxylate (430 mg, 1.30 mmol) in tetrahydrofuran is treated with NaH (60% in mineral oil, 78 mg, 1.95 mmol) portion-wise under nitrogen at room temperature, stirred for 0.5 hr, treated with benzenesulfonyl chloride (0.25 ml, 1.95 mmol), stirred for 17 hr under nitrogen at room temperature, quenched with ice-water and diluted with ethyl acetate. The phases are separated and the aqueous phase is extracted with ethyl acetate. The combined extracts and organic phase are washed with water and saturated NaCl, dried over MgSO4 and concentrated in vacuo. The resultant residue is purified by flash chromatography (silica gel, EtOAc/hexane, 1/9) to afford the title compound as a yellow solid, 350 mg, mp 63-65° C., identified by NMR and mass spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613781B2
Source datasetuspto-grants-2003_09
ORD IDord-3d07f12a7b644716b0349328659bd029
Source noteuspto-grants-2003_09