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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022665Generated: October 26, 2026

Water → tert-butyl (6SR,7SR)-7-(3,4-dichlorophenyl)-6-[(methylsulfonyl)amino]-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022665

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactanttert-butyl (6SR,7SR)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 66975299—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (6SR,7SR)-7-(3,4-dichlorophenyl)-6-[(methylsulfonyl)amino]-1,4-oxazepane-4-carboxylateHCID 6697603382.2%

Reaction Steps

Methanesulfonyl chloride (34 mg) was added to a solution of tert-butyl (6SR,7SR)-6-amino-7-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (90 mg) and triethylamine (33 mg) in THF (5 mL), and the mixture was stirred at room temperature for 1 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (90 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-870da08f2e68436e8367b1e693122630
Source noteuspto-grants-2014_05