HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361441Generated: October 31, 2026
m-Chloroperbenzoic acid → HCID 21186241, compound
https://huagongshe.com/reaction/361441
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | HCID 21186230 | HCID 21186230 | — |
| Product | HCID 21186241 | HCID 21186241 | 8.6% |
Reaction Steps
3-Chloroperoxybenzoic acid (50%, 2.4 g) was added over 5 minutes to a solution of N-(isobutoxycarbonyl)-N-(3-methoxy-5-methylpyrazin-2-yl)-2-[4-(2-methylprop-2-enyl)phenyl]pyridine-3-sulphonamide (1.8 g) in dichloromethanc (75 ml) at 0° C. The reaction mixture was allowed to warm to ambient temperature and stirred a further 1 hour. The mixture was washed with saturated aqueous sodium hydrogen carbonate solution (20 ml), water and saturated sodium chloride solution then dried (MgSO4). Volatile material was removed by evaporation and the residue was purified by suction flash chromatography followed by gradient elution with 0-40% ethyl acetate/hexane through a silica gel Mega Bond Elut column to give 2-[4-(2,3-epoxy-2-methylpropyl)phenyl]-N-(isobutoxycarbonyl)-N-(3-methoxy-5-methylpyrazin-2-yl)pyridine-3-sulphonamide (0.16 g) as a solid, 1H NMR (CDCl3): 0.65 (d, 6 H), 1.3 (s, 3 H), 1.7 (m, 1 H), 2.5 (s, 3 H), 2.65 (dd, 2 H), 2.9 (q, 2 H), 3.85 (d, 2 H), 4.0 (s, 3 H), 7.3 (d, 2 H), 7.5 (dd, 1 H), 7.6 (d, 2 H), 7.95 (s, 1 H), 8.85 (dd, 1 H), 8.95 (dd, 1 H); mass spectrum (+ve ESP): 527 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866568 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-ad3e75984655428c92bac8f83ccaacee |
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| Source note | uspto-grants-1999_02 |
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