돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 216648생성일: 2026년 10월 25일

Methanesulfonic Acid → (2R)-2-phenylcarbonyloxypropyl (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoate mesylate

https://huagongshe.com/reaction/216648

반응식

참여 물질

역할이름HCID투입량
반응물Methanesulfonic AcidHCID 6395—
반응물tert-Butyl methyl etherHCID 15413—
반응물(2R)-2-Phenylcarbonyloxypropyl(2S)-2-(tert-Butoxycarbonyl)amino-3-(3,4-dihydroxyphenyl)propanoateHCID 46899463—
용매1,4-DioxaneHCID 31275—
생성물(2R)-2-phenylcarbonyloxypropyl (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoate mesylateHCID 1612513454.4%

반응 단계

Methanesulfonic acid (3.9 mL, 60.1 mmol) was slowly added to a solution of (2R)-2-phenylcarbonyloxypropyl (2S)-2-(tert-butoxycarbonyl)amino-3-(3,4-dihydroxyphenyl)propanoate 2 (11.0 g, 22.1 mmol) in 1,4-dioxane (30 mL) while stirred at room temperature. The reaction mixture was stirred for 2 h. The solution was slowly added to methyl tert-butyl ether (MTBE) (600 mL) with vigorous stirring. The resulting suspension was filtered. The filter cake was washed three times with methyl tert-butyl ether and air dried to afford 5.48 g (54% yield) of the mesylate salt 1 as an off-white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08193242B2
출처 데이터셋uspto-grants-2012_06
ORD IDord-9d4102aa4648481fb3d051f2e028eb85
출처 메모uspto-grants-2012_06