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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyrrolidine | HCID 31268 | — |
| 반응물 | Potassium Bromide | HCID 253877 | — |
| 반응물 | 2-(Chloromethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)-aminocarbonyl]benzenesulfonamide | HCID 13364617 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-(1-Pyrrolidinylmethyl)-N-[(4,6-dimethoxypyrimidin-2-yl)aminocarbonyl]benzenesulfonamide, hydrochloride salt | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04723990 |
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| 출처 데이터셋 | uspto-grants-1988_02 |
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| ORD ID | ord-849b814f85c74b4ea52ba55f26ec47fb |
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| 출처 메모 | uspto-grants-1988_02 |
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