홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Potassium Carbonate → Rasagiline

HRID 401851
노트
인쇄 미리보기

반응식

HRID 401851 반응식
[CH:1]#[C:2][CH2:3][NH:4][C@H:5]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH2:7][CH2:6]1.Cl.C(Cl)C#C.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[CH:1]#[C:2][CH2:3][NH:4][C@H:5]1[C:13]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[CH2:7][CH2:6]1
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 122213-Chloro-1-propyneHCID 9794292Rasagiline hydrochloride

생성물 1

HCID 3052776Rasagiline수율 56%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

Another process for preparation of Rasagiline hydrochloride as disclosed in EP '492 comprises reaction of R(−)-1-aminoindan (8) with propargyl chloride (6) in presence of potassium carbonate in acetonitrile (ACN) at 60° C. for 16 hours to obtain R(+) Rasagiline base (9) which is then purified by column chromatography. The purified base is then converted to R(+)-Rasagiline hydrochloride followed by recrystallization with isopropanol. The main disadvantage of this process is longer reaction time (16 hours) and low overall yield of about 56%.

출처 및 근거

ORD 기록
ord-07d03e85e0ac476bb65c4f60769aa0a2
출처 데이터셋
uspto-grants-2014_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08741962B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트