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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018469Generated: November 1, 2026

Triethylamine → HCID 9953707, compound

https://huagongshe.com/reaction/1018469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-Acetylsulfanilyl chlorideHCID 8481—
ReactantHCID 18401525HCID 18401525—
SolventDichloromethaneHCID 6344—
ProductHCID 9953707HCID 9953707—

Reaction Steps

To a stirred suspension of 4-N-acetylsulphanilyl chloride (2.7 g, 11.55 mmol) and triethylamine (1.95 g, 19.25 mmol) in dichloromethane (50 ml) was added portionwise solid 3,6-dihydro-3,5-dimethyl-6-(4-methoxyphenyl)-2H-1,2-oxazine hydrochloride (1.97 g, 7.70 mmol). The resulting solution was stirred at room temperature for 5 h then washed with water three times, aqueous sodium hydroxide (2M), water and brine. The organic phase was dried over magnesium sulphate, filtered and evaporated, the resulting foam was purified on flash silica eluting with ethylacetate-hexane (3:2) to give 2-(4-acetamidobenzenesulphonyl)-3,6-dihydro-3,5-dimethyl-6-(4-methoxyphenyl)-2H-1,2-oxazine as a white foam. 1H NMR (CDCl3) δ 1.39(3H,s), 1.41(3H, d), 2.20(3H, s), 3.79(3H, s), 4.45(1H, m), 5.19(1H, s), 5.68(1H, d), 6.80(2H, d), 7.13(2H, d), 7.57(1H, bs), 7.59(2H, d), 7.80(2H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06482824B1
Source datasetuspto-grants-2002_11
ORD IDord-06e647e335804ae781fc6380e814ac72
Source noteuspto-grants-2002_11