Cysteamine Hydrochloride → 2-[(4-Methyl-1,2,5-oxadiazol-3-yl)methylthio]ethylamine
반응식
O[CH2:2][C:3]1[C:7]([CH3:8])=[N:6][O:5][N:4]=1.Cl.[NH2:10][CH2:11][CH2:12][SH:13]>Br>[CH3:8][C:7]1[C:3]([CH2:2][S:13][CH2:12][CH2:11][NH2:10])=[N:4][O:5][N:6]=1참가 물질
4
실험 절차
A solution of 3-hydroxymethyl-4-methylfurazan (2.49 g; 21.8 mmoles) [prepared in Step A] and 2-aminoethanethiol hydrochloride (2.48 g; 21.8 mmoles) in 60 ml of 48% aqueous hydrobromic acid was stirred and heated at reflux temperature for 23 hours and then at ambient temperature for 40 hours. The excess hydrobromic acid was removed under reduced pressure, and the oil residue was dissolved in isopropyl alcohol, filtered through Celite and the product was crystallized from the filtrate. Recrystallization from isopropyl alcohol yielded the title compound as the hydrobromide salt, mp 142°-143°.
후처리
- temperatureheated
- temperatureat reflux temperature for 23 hours
- customThe excess hydrobromic acid was removed under reduced pressure
- dissolutionthe oil residue was dissolved in isopropyl alcohol
- filtrationfiltered through Celite
- customthe product was crystallized from the filtrate
- customRecrystallization from isopropyl alcohol
출처 및 근거
- ORD 기록
- ord-fdb4cb2bde4f4b39a843095a6ad22ff6
- 출처 데이터셋
- uspto-grants-1983_07
- 특허 번호
- US04394508
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