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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | 2-Chloro-4-methylpyrimidine | HCID 11629607 | — |
| Reactant | Ethyl 3-{[(2,6-difluorophenyl)sulfonyl]amino}-4-fluorobenzoate | HCID 57989990 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-{5-[(2-Chloro-4-pyrimidinyl)acetyl]-2-fluorophenyl}-2,6-difluorobenzenesulfonamide | HCID 57989679 | 50% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994185B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-23a257e4bc6b4732a5b8b785cbf31b04 |
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| Source note | uspto-grants-2011_08 |
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