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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224081Generated: November 1, 2026

Water → 7-Benzenesulfonyl-4-(1-benzyl-pyrrolidin-3-yl)-3,4-dihydro-2H-benzo[1,4]oxazine

https://huagongshe.com/reaction/2224081

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactant1-Benzylpyrrolidin-3-yl methanesulfonateHCID 9899811—
Reactant7-benzenesulfonyl-3,4-dihydro-2H-benzo[1,4]oxazineHCID 58641513—
SolventDimethylformamideHCID 6228—
Product7-Benzenesulfonyl-4-(1-benzyl-pyrrolidin-3-yl)-3,4-dihydro-2H-benzo[1,4]oxazineHCID 5864152040.2%

Reaction Steps

To a suspension of sodium hydride (0.033 g. of a 60% dispersion in mineral oil, 0.834 mmol) in 3 mL dimethylformamide was added portionwise 7-benzenesulfonyl-3,4-dihydro-2H-benzo[1,4]oxazine (0.200 g, 0.726 mmol), and the resulting suspension was stirred at room temperature for 10 minutes. Racemic methanesulfonic acid 1-benzyl-pyrrolidin-3-yl ester (0.259 g., 1.018 mmol) was added dropwise and the reaction mixture was heated to 65° C. for 21 hours. The reaction mixture was then poured into 100 mL water, and extracted three times with 50 mL ethyl acetate. The organic fraction was washed twice with 50 mL 10% aq. hydrogen chloride and once with 50 mL saturated sodium bicarbonate. The organic fraction was then dried over sodium sulfate and concentrated in vacuo. The crude product was purified by flash chromatography (2%-5% methanol in dichlormethane) to give 0.127 g (0.292 mmol, 40%) of 7-benzenesulfonyl-4-(1-benzyl-pyrrolidin-3-yl)-3,4-dihydro-2H-benzo[1,4]oxazine as a red oil. MS: 474 (M+ACN)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378415B2
Source datasetuspto-grants-2008_05
ORD IDord-32b9d76836cc4441b31987bb37a3e318
Source noteuspto-grants-2008_05