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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 4138생성일: 2026년 10월 24일

Pyrrolidine → 2-(1-Pyrrolidinylmethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]benzenesulfonamide, hydrochloride salt

https://huagongshe.com/ko/reaction/4138

반응식

참여 물질

역할이름HCID투입량
반응물PyrrolidineHCID 31268—
반응물Potassium BromideHCID 253877—
반응물2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamideHCID 13364617—
용매DimethylformamideHCID 6228—
생성물2-(1-Pyrrolidinylmethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]benzenesulfonamide, hydrochloride saltHCID 13364619—

반응 단계

A slurry of 2-(chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]benzenesulfonamide (1.00 g) in dimethylformamide (5 ml) was contacted with pyrrolidine (0.45 ml) and stirred for 3.5 hrs. Volatiles were removed under vacuum and the residue was taken up in methanol. Solvent was removed and the water (15 ml) was added and the pH was adjusted to 6.0 by addition of dilute hydrochloric acid. Cooling and scratching produced a white solid which was collected and dried to give 488 mg, m.p. 117°-123°. A 400 mg sample was crystallized from acetonitrile to give 269 mg. m.p. 132°-134° C. 1H nmr δCDCl3TMS 13.0-11.0 (brds 2H), 8.63 (s, 1 NH), 8.37-8.20, 8.05-7.90, and 7.70-7.33 (m, 4H), 5.68 (s, 1H), 5.00 (s, 2H), 3.90 (s, 6H), 3.70-2.90 (m, 4H), 2.30-1.90 (m, 4H). IR (KBr) 3650-2200, 1710, 1610, 1580, 1450, 1360, 1200, 1165 are major absorption bands.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04723990
출처 데이터셋uspto-grants-1988_02
ORD IDord-849b814f85c74b4ea52ba55f26ec47fb
출처 메모uspto-grants-1988_02