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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 256538생성일: 2026년 10월 26일

Methyl Methanesulfonate → 1-(2-Hydroxyethyl)-2-methylthio-3,4,5,6-tetrahydropyrimidine mesylate

https://huagongshe.com/reaction/256538

반응식

참여 물질

역할이름HCID투입량
반응물Methyl MethanesulfonateHCID 4156—
반응물1-(2-Hydroxyethyl)-3,4,5,6-tetrahydropyrimidine-2-thioneHCID 3603281—
용매EthanolHCID 702—
용매tert-Butyl methyl etherHCID 15413—
생성물1-(2-Hydroxyethyl)-2-methylthio-3,4,5,6-tetrahydropyrimidine mesylateHCID 86747344128.8%

반응 단계

Then, 1-(2-hydroxyethyl)-3,4,5,6-tetrahydropyrimidine-2-thione (121.2 g) and methyl methanesulfonate (91.51 g) are heated at reflux in ethyl alcohol (200 ml) for about 2 hours and then allowed to cool to room temperature. The mixture was diluted with t-butyl methyl ether (2 liters). An oil separates which crystallizes on keeping in freezer at -20° C. Filtration and drying yields 145.7 g of 1-(2-hydroxyethyl)-2-methylthio-3,4,5,6-tetrahydropyrimidine mesylate, melting point 61.7°-62.2° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05258381
출처 데이터셋uspto-grants-1993_11
ORD IDord-333625bfe3524323baec2a941c41e1f7
출처 메모uspto-grants-1993_11