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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1022791Generated: October 25, 2026

Water → tert-butyl (6SR,7RS)-6-(3,4-dichlorophenyl)-7-{[(phenylsulfonyl)amino]methyl}-1,4-oxazepane-4-carboxylate

https://huagongshe.com/reaction/1022791

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactanttert-butyl (6RS,7SR)-7-(aminomethyl)-6-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylateHCID 66975190—
SolventTetrahydrofuranHCID 8028—
Producttert-butyl (6SR,7RS)-6-(3,4-dichlorophenyl)-7-{[(phenylsulfonyl)amino]methyl}-1,4-oxazepane-4-carboxylateHCID 6697655151.4%

Reaction Steps

Benzenesulfonyl chloride (130 mg) was added dropwise to a solution of tert-butyl (6SR,7RS)-7-(aminomethyl)-6-(3,4-dichlorophenyl)-1,4-oxazepane-4-carboxylate (280 mg) and triethylamine (0.14 mL) 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 (195 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722662B2
Source datasetuspto-grants-2014_05
ORD IDord-eff4c15539f64ff8820a2da886d68a1d
Source noteuspto-grants-2014_05