HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362956Generated: October 29, 2026
Methanesulfonyl chloride → HCID 58964299, compound
https://huagongshe.com/reaction/1362956
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 58964273 | HCID 58964273 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 58964299 | HCID 58964299 | 35.6% |
Reaction Steps
N-[4-[2-(4-Amino-piperidin-1-yl)-ethoxy]-3-(4-chloro-2-methyl-2H-pyrazol-3-yl)-phenyl]-3-trifluoromethyl-benzamide (0.038 g, 0.073 mmol) was dissolved in DMA (2.0 mL) in a vial with stir bar. Methanesulfonyl chloride (0.0085 g, 0.11 mmol) was added and the reaction was stirred at rt overnight. The reaction was concentrated, added to NaHCO3 (5 mL), and the solution was extracted with EtOAc (2×20 mL). The organic extracts were dried (Na2SO4), filtered, concd and purified by prep HPLC to afford the title compound (0.016 g, 0.026 mmol, 35%, TFA salt) as a white solid. LCMS m/z (%)=600 (M+H35Cl, 100), 602 (M+H37Cl, 36). 1H NMR (400 MHz, DMSO-d6) δ: 10.54 (s, 1H), 9.30 (s, 1H), 8.30 (s, 1H), 8.26 (d, J=8.0 Hz, 1H), 7.97 (m, 2H), 7.80 (m, 1H), 7.72 (d, J=2.6 Hz, 1H), 7.68 (s, 1H), 7.31 (m, 1H), 4.40 (m, 1H), 4.32 (m, 1H), 3.69 (s, 3H), 3.50-2.90 (m, 7H), 2.95 (s, 3H), 2.00-1.50 (m, 4H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07884101B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-bd41c389010b43179f8edf318bbd5ae1 |
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| Source note | uspto-grants-2011_02 |
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