HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353879Generated: October 31, 2026
Pyridine → Isopropyl 5-[acetyl-(3,5-bistrifluoromethylbenzyl)amino]-8-methanesulfonylamino-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate
https://huagongshe.com/reaction/2353879
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Isopropyl 5-[acetyl-(3,5-bistrifluoromethylbenzyl)amino]-8-amino-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate | HCID 59003104 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Isopropyl 5-[acetyl-(3,5-bistrifluoromethylbenzyl)amino]-8-methanesulfonylamino-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate | HCID 59003125 | 58.6% |
Reaction Steps
Add methanesulfonyl chloride (13 μl, 0.170 mmol) dropwise to a suspension of isopropyl-5-[acetyl-(3,5-bistrifluoromethylbenzyl)amino]-8-amino-2,3,4,5-tetrahydrobenzo[b]azepine-1-carboxylate (0.082 g, 0.154 mmol) and pyridine (15 μl, 0.185 mmol) in dichloromethane (2 mL) at 0° C. under nitrogen. Stir the orange suspension for 0.5 h, then remove the cooling bath and warm the mixture to room temperature and stir overnight. Dilute the mixture with dichloromethane (30 mL) and wash with 2 N HCl, water and brine (10 mL each), then dry the organic layer over sodium sulfate, filter and remove the solvent under reduced pressure. Purify the residue using chromatography on silica gel, eluting with ethyl acetate/hexanes (70:30), to provide the title compound as a white solid (0.055 g, 58%): ESI MS 610 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07749992B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-5870b0f5078f47ff905fa472d9099a6a |
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| Source note | uspto-grants-2010_07 |
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