HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094351Generated: November 2, 2026
Methanesulfonyl chloride → HCID 58007547, compound
https://huagongshe.com/reaction/1094351
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 66637156 | HCID 66637156 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58007547 | HCID 58007547 | 96.6% |
Reaction Steps
A solution of (S)-2-amino-N-(3,4-dimethyl-phenyl)-2-phenyl-N-[2-(6-trifluoromethyl-pyridin-3-yl)-ethyl]-acetamide hydrochloride (40 mg, 0.086 mmol, derived from example 1) in dry CH2Cl2 (1.5 mL) was treated with methanesulphonyl chloride (10 mg, 0.087 mmol) under Argon and the mixture stirred at ambient temperature for 30 min then quenched with aqueous Na2CO3 (2 M, 1 mL), concentrated, then redissolved in EtOAc (15 mL) and washed with aqueous Na2CO3 (2 M, 3×15 mL). The combined aqueous layers were extracted with EtOAc (15 mL) and the combined organic layers dried over sodium sulfate. Concentration and purification by chromatography (SiO2, heptane:ethyl acetate=95:5 to 60:40) afforded the title compound (42 mg, 96%) as a light yellow oil. MS m/e: 506.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08133909B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-56c8303466404835a3bd7d7ef5d48a13 |
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| Source note | uspto-grants-2012_03 |
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