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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670939Generated: October 26, 2026

Lithium Hexamethyldisilazide → N-{5-[(2-Chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide

https://huagongshe.com/reaction/1670939

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant2-Chloro-4-methylpyrimidineHCID 11629607—
ReactantEthyl 3-{[(2,6-difluorophenyl)sulfonyl]amino}-4-fluorobenzoateHCID 57989990—
SolventTetrahydrofuranHCID 8028—
ProductN-{5-[(2-Chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamideHCID 5798967950%

Reaction Steps

To a solution of ethyl 3-{[(2,6-difluorophenyl)sulfonyl]amino}-4-fluorobenzoate (5.0 g, 13.9 mmol) in THF (100 mL) was added 1.0 M LiHMDS in THF (34.8 mL, 34.8 mmol). A solution of 2-chloro-4-methylpyrimidine (2.7 g, 20.9 mmol) in THF (100 mL) was added dropwise over 30 min, and the reaction was stirred overnight at rt. The reaction was quenched with 10 mL of MeOH and concentrated, and the residue was partitioned between EtOAc and saturated aqueous NaHCO3. The aqueous layer was extracted with 2×50 mL EtOAc, and the combined organic layers were passed through a pad of silica gel, concentrated, and adsorbed onto silica gel. The crude product was purified via flash chromatography with 0-100% EtOAc/DCM to generate 3.07 g (50% yield) of the title compound as a white powder. MS (ESI): 443 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994185B2
Source datasetuspto-grants-2011_08
ORD IDord-23a257e4bc6b4732a5b8b785cbf31b04
Source noteuspto-grants-2011_08