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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 573697Generated: October 30, 2026

(4-Chlorophenyl)methanesulfonyl chloride → HCID 68323916, compound

https://huagongshe.com/reaction/573697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Chlorophenyl)methanesulfonyl chlorideHCID 227304—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 68323863HCID 68323863—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68323916HCID 6832391613.2%

Reaction Steps

To a stirred solution of 2,6-dimethyl-3-[3-(methyloxy)phenyl]thieno[2,3-b]pyridin-4-amine (100 mg, 0.352 mmol) (Description 4) in THF (2 mL) cooled in an ice bath was added LiHMDS (1M solution in THF) (0.774 mL, 0.774 mmol). The reaction mixture was stirred at RT for 45 min before the addition of 4-chlorobenzylsulfonyl chloride (198 mg, 0.879 mmol). The reaction mixture was then stirred at RT for a further 16 h and was then cooled in an ice bath before the addition of LiHMDS (1M solution in THF) (0.352 mL, 0.352 mmol). The reaction mixture was stirred at RT for 1 h before the addition of 4-chlorobenzylsulfonyl chloride (79.2 mg, 0.352 mmol). The reaction mixture was stirred at RT for a further 16 h and then diluted with water (10 mL) and the aqueous layer extracted with DCM (3×20 mL). The combined organic extracts were dried over a phase separating column and concentrated. The residue was purified by MDAP (basic conditions), to afford the title compound (22 mg). LCMS (A) m/z: 473 [M+1]+, Rt 1.42 min (basic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029545B2
Source datasetuspto-grants-2015_05
ORD IDord-55a5462831054be58e18d367d90ded9c
Source noteuspto-grants-2015_05