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

Sulfuric Acid → HCID 131730603, 화합물

HRID 2098312
노트
인쇄 미리보기

반응식

HRID 2098312 반응식
[CH3:1][CH:2]1[S:13][CH2:12][C:4]2([CH:9]3[CH2:10][CH2:11][N:6]([CH2:7][CH2:8]3)[CH2:5]2)[O:3]1.[S:14](=[O:18])(=[O:17])([OH:16])[OH:15]>C1(C)C=CC=CC=1>[CH3:1][CH:2]1[S:13][CH2:12][C:4]2([CH:9]3[CH2:10][CH2:11][N:6]([CH2:7][CH2:8]3)[CH2:5]2)[O:3]1.[S:14]([O-:18])([O-:17])(=[O:16])=[O:15]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 1118Sulfuric AcidHCID 2684Evoxac

생성물 1

HCID 131730603HCID 131730603, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

반응 조건

온도
2.5 °C

실험 절차

Charged toluene (50 ml) and to this charged cevimeline free base with cis isomer >90% (5.0 g) (prepared by any one of the above methods given in examples III to V). Stirred for 10 to 15 minutes to obtain a clear solution. Cooled the solution to 0 to 5° C. Charged concentrated sulfuric acid (1.3 ml) drop wise over 30 minutes and stir the resultant liberated sulfate salt for 30 minutes at 0 to 5° C. Then slowly raised the temperature to reflux temperature (100 to 115° C.) and continued the reflux for 60 to 90 minutes. The reaction mass was then cooled and processed as in Example VI to yield 3.5 g of cevimeline sulfate with cis isomer >97% purity by HPLC.

후처리

  1. customto obtain a clear solution
  2. stirringstir the resultant
  3. customfor 30 minutes
  4. customat 0 to 5° C
  5. temperatureThen slowly raised the temperature
  6. temperatureto reflux temperature (100 to 115° C.)
  7. temperaturereflux for 60 to 90 minutes
  8. temperatureThe reaction mass was then cooled

출처 및 근거

ORD 기록
ord-9536e292e0f648cda83d39d9c64f42ed
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08450487B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트