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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1427880Generated: November 2, 2026

Sulfamide → (S)-3-((4-methoxybenzyl)oxy)pyrrolidine-1-sulfonamide

https://huagongshe.com/reaction/1427880

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamideHCID 82267—
Reactant(S)-3-((4-methoxybenzyl)oxy)pyrrolidineHCID 86325453—
Solvent1,2-DimethoxyethaneHCID 8071—
Product(S)-3-((4-methoxybenzyl)oxy)pyrrolidine-1-sulfonamideHCID 8670290561.2%

Reaction Steps

A mixture of (S)-3-((4-methoxybenzyl)oxy)pyrrolidine (4.50 g, 21.7 mmol) and sulfamide (2.50 g, 26.0 mmol) in dimethoxyethane (100 mL) was refluxed for 72 h. The reaction was concentrated in vacuo. Purification of the residue by column chromatography (30% to 100% gradient ethyl acetate in hexanes) afforded the title compound as a colorless solid (3.80 g, 61%): 1H NMR (300 MHz, DMSO-d6) δ 7.27-7.24 (m, 2H), 6.91-6.88 (m, 2H), 6.74 (s, 2H), 4.39 (s, 2H), 4.16-4.11 (m, 1H), 3.74 (s, 3H), 3.30-3.25 (m, 1H), 3.18-3.10 (m, 3H), 2.00-1.88 (m, 2H); MS (ES+) m/z 287.2 (M+1); MS (ES−) m/z 285.3 (M−1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08933236B2
Source datasetuspto-grants-2015_01
ORD IDord-57f7e36752de4052a9250a2cbc3b8c11
Source noteuspto-grants-2015_01