Tetrahydrofuran → 3-(Cyclobutylamino)propane-1-sulfonic acid
반응식
[CH:1]1([NH2:5])[CH2:4][CH2:3][CH2:2]1.[CH2:6]1[CH2:12][S:9](=[O:11])(=[O:10])[O:8][CH2:7]1.C1COCC1>C(#N)C>[CH:1]1([NH:5][CH2:7][CH2:6][CH2:12][S:9]([OH:11])(=[O:10])=[O:8])[CH2:4][CH2:3][CH2:2]1참가 물질
실험 절차
A mixture of cyclobutylamine (1.11 g, 15.6 mmol) and 1,3-propane sultone (2 g, 17 mmol) in acetonitrile (18 mL) was heated at reflux. The mixture turned to a lump within 15 minutes. THF (10 mL) was added. The reflux was maintained for 1 hour. The mixture was cooled to room temperature. The solid was collected by filtration, rinsed with acetonitrile (2×4 mL), air-dried for 60 minutes (2.41 g). The solid was suspended in methanol (20 mL) and the suspension was heated at reflux until all the solid material was dissolved. The mixture was then cooled to room temperature. The solid thus formed was collected by suction filtration, rinsed with methanol (2×4 mL), air-dried for 20 minutes, and further dried in a vacuum oven at 40° C. for 18 hours. Compound EC was obtained as a white solid (1.81 g, 60% yield). 1H NMR (500 MHz, D2O) δ 1.70-1.77 (m, 2H), 1.94-2.03 (m, 4H), 2.18 (br s, 2H), 2.85 (t, J=6.8 Hz, 1H), 2.95 (t, J=7.3 Hz, 1H), 3.63-3.66 (m, 1H). 13C NMR (125 MHz, D2O) δ 14.5, 21.5, 26.1, 43.6, 48.0, 51.8. ES-MS 194 (M+1).
후처리
- temperaturewas heated
- temperatureat reflux
- temperatureThe reflux was maintained for 1 hour
- filtrationThe solid was collected by filtration
- washrinsed with acetonitrile (2×4 mL)
- customair-dried for 60 minutes (2.41 g)
- temperaturethe suspension was heated
- temperatureat reflux until all the solid material
- dissolutionwas dissolved
- temperatureThe mixture was then cooled to room temperature
- customThe solid thus formed
- filtrationwas collected by suction filtration
- washrinsed with methanol (2×4 mL)
- customair-dried for 20 minutes
- customfurther dried in a vacuum oven at 40° C. for 18 hours
출처 및 근거
- ORD 기록
- ord-891f548053204af48cd80d62c0ee5c00
- 출처 데이터셋
- uspto-grants-2014_02
- 특허 번호
- US08642801B2
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