HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1946313Generated: October 30, 2026
Ammonium Chloride → Methyl 4-chloro-3-[(3-{[(2,6-difluorophenyl)carbonyl]amino}-1H-pyrazol-1-yl)methyl]benzoate
https://huagongshe.com/reaction/1946313
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| Reactant | Methyl 3-(bromomethyl)-4-chlorobenzoate | HCID 12144656 | — |
| Reactant | HCID 178522346 | HCID 178522346 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | HCID 68569164 | HCID 68569164 | — |
| Product | Methyl 4-chloro-3-[(3-{[(2,6-difluorophenyl)carbonyl]amino}-1H-pyrazol-1-yl)methyl]benzoate | HCID 59547941 | — |
Reaction Steps
1.0 M LiHMDS (5.00 ml, 5.00 mmol) in THF/ethylbenzene was added slowly to a solution of 2,6-difluoro-N-(1H-pyrazol-3-yl)benzamide (for a preparation see Intermediate 9)(1.12 g, 5 mmol) in THF (50 ml) under nitrogen at ambient temperature. The solution was stirred for 20 min and a solution of methyl 3-(bromomethyl)-4-chlorobenzoate (1.32 g, 5.0 mmol, synthesised according to WO2006079857) in THF (4 ml) was added in one portion. The solution was stirred for 2 h and left overnight. The solution was treated with aqueous ammonium chloride (50 ml) and extracted with ethyl acetate (2×50 ml). The combined organic extracts were dried (Na2SO4), filtered and solvent evaporated in vacuo. The residue was purified on a silica cartridge (50 g) eluted with 0-100% cyclohexane/EtOAc to give the title compound (1.95 g) as a white solid after evaporation from diethyl ether; LCMS: (System 4) MH+=406/408, tRET=2.69 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399436B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-cd2407bba64045388dbbd2330cbafdc9 |
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| Source note | uspto-grants-2013_03 |
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