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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 877535생성일: 2026년 10월 24일

Methanol → (5-(6-Chloro-4-(isopropylamino)pyridin-3-yl)-1,3,4-thiadiazol-2-yl)(3-(hydroxymethyl)pyrrolidin-1-yl)methanone

https://huagongshe.com/ko/reaction/877535

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물L-ProlinolHCID 640091—
반응물Methyl 5-(6-chloro-4-(isopropylamino)pyridin-3-yl)-1,3,4-thiadiazole-2-carboxylateHCID 89690804—
생성물(5-(6-Chloro-4-(isopropylamino)pyridin-3-yl)-1,3,4-thiadiazol-2-yl)(3-(hydroxymethyl)pyrrolidin-1-yl)methanoneHCID 89691050—

반응 조건

온도80 °C

반응 단계

To a stirred solution of methyl 5-(6-chloro-4-(isopropylamino)pyridin-3-yl)-1,3,4-thiadiazole-2-carboxylate (12) (60 mg, 0.1 mmol) in MeOH (2 mL), (S)-Prolinol (0.9 mmol, 5 equiv) was added and refluxed at 80° C. for 1 h. The reaction mixture was cooled and concentrated. The crude material obtained was purified by column chromatography through silica gel and MeOH: DCM as eluent to isolate the desired product, (5-(6-chloro-4-(isopropylamino)pyridin-3-yl)-1,3,4-thiadiazol-2-yl)(3-(hydroxymethyl)pyrrolidin-1-yl)methanone ( ). LCMS: XBridge Phe 8, 4.6×30 mm, 3.5 μm; Solvent A=2% ACN: 98% H2O: 10 mM NH4COOH; Solvent B=98% ACN: 2% H2O: 10 mM NH4COOH; gradient 0-100% B over 1.5 min (3.2 min run time); retention time: 1.585 min; LCMS (ES-API), m/z 379.8 (M−H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987311B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-20ec6a18584e4619b5f935a8e1624bf6
출처 메모uspto-grants-2015_03