Hydrochloric Acid → (S)-1-(5-(5-(cyclopropylmethylthio)-3-(2-methylpyridin-3-yloxy)-pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)ethane-1,2-diol
반응식
[CH:1]1([CH2:4][S:5][C:6]2[CH:7]=[C:8]([O:28][C:29]3[C:30]([CH3:35])=[N:31][CH:32]=[CH:33][CH:34]=3)[C:9]([NH:12][C:13]3[S:17][N:16]=[C:15]([C@H:18]4[CH2:22][O:21]C5(CCCCC5)[O:19]4)[N:14]=3)=[N:10][CH:11]=2)[CH2:3][CH2:2]1.Cl>C(O)C>[CH:1]1([CH2:4][S:5][C:6]2[CH:7]=[C:8]([O:28][C:29]3[C:30]([CH3:35])=[N:31][CH:32]=[CH:33][CH:34]=3)[C:9]([NH:12][C:13]3[S:17][N:16]=[C:15]([C@H:18]([OH:19])[CH2:22][OH:21])[N:14]=3)=[N:10][CH:11]=2)[CH2:3][CH2:2]1참가 물질
4
반응물 2
생성물 1
시약·촉매·용매 1
반응 조건
- 온도
- 80 °C
실험 절차
To a solution of (S)-N-(5-(cyclopropylmethylthio)-3-(2-methylpyridin-3-yloxy)-pyridin-2-yl)-3-(1,4-dioxaspiro[4.5]decane-2-yl)-1,2,4-thiadiazol-5-amine (0.30 g, 0.586 mmol) in ethanol (20 mL) was added 1 M HCl (0.87 mL) and the reaction heated to 80° C. for 2 hours. The reaction was cooled and concentrated in vacuo and the solid triturated with ethanol The solid was dried in vacuo to afford (S)-1-(5-(5-(cyclopropylmethylthio)-3-(2-methylpyridin-3-yloxy)-pyridin-2-ylamino)-1,2,4-thiadiazol-3-yl)ethane-1,2-diol (0.146 g, 0.338 mmol, 57.7% yield) as the mono HCl salt. Mass Spectrum (apci) m/z=432.0 (M+H−HCl).
후처리
- temperatureThe reaction was cooled
- concentrationconcentrated in vacuo
- customthe solid triturated with ethanol The solid
- customwas dried in vacuo
출처 및 근거
- ORD 기록
- ord-5cf36c745bd34df4b06d621aa2b30959
- 출처 데이터셋
- uspto-grants-2014_10
- 특허 번호
- US08853409B2
반응 노트
불러오는 중…