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

Ethanol → Napactadine Hydrochloride

HRID 1449128
노트
인쇄 미리보기

반응식

HRID 1449128 반응식
[ClH:1].[CH:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[CH2:12][C:13](=[NH:17])OCC.[CH3:18][NH2:19].[CH2:20](O)C>>[ClH:1].[CH3:18][NH:19][C:13](=[N:17][CH3:20])[CH2:12][C:3]1[CH:4]=[CH:5][C:6]2[C:11](=[CH:10][CH:9]=[CH:8][CH:7]=2)[CH:2]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 702EthanolHCID 6329MethylamineHCID 20349999HCID 20349999, 화합물

생성물 1

HCID 16072198Napactadine Hydrochloride수율 85%

반응 조건

온도
2 °C

실험 절차

In a 100 ml. reaction vessel, equipped with a stirrer, thermometer, a pressure-equalizing addition funnel, and a reflux condenser fitted with a drying tube, 11.95 grams (0.048 mol.) of ethyl 2-naphthaleneethanimidate hydrochloride was placed. A solution of 21.20 grams (0.683 mol.) of methylamine in 35 ml. of absolute ethanol was rapidly added to the reaction mixture. The temperature quickly rose to 65° C. and dropped to about 30° C. after all of the solution was added. The reaction mixture was kept between about 50°-53° C. for 21 hours. The reaction mixture was cooled to 2° C. and the white crystalline product was filtered off. The product was washed with toluene and dried to give 10.2 grams (85% yield) of the title compound. The crude product was recrystallized from absolute ethanol to yield 8.97 grams of the title compound. The melting point was 225.5°-227° C.

후처리

  1. customreaction vessel
  2. customequipped with a stirrer
  3. additionthermometer, a pressure-equalizing addition funnel, and a reflux condenser
  4. customfitted with a drying tube
  5. customquickly rose to 65° C.
  6. additiondropped to about 30° C. after all of the solution
  7. additionwas added
  8. filtrationthe white crystalline product was filtered off
  9. washThe product was washed with toluene
  10. customdried

출처 및 근거

ORD 기록
ord-006c3b81a4b544d6872fd1d8574199f7
출처 데이터셋
uspto-grants-1980_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04189444

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트