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

Trifluoroacetic acid → 4-Carbamoyl-1,2,3,6-tetrahydropyridine trifluoroacetate

HRID 2182058
노트
인쇄 미리보기

반응식

HRID 2182058 반응식
C(OC([N:8]1[CH2:13][CH:12]=[C:11]([C:14](=[O:16])[NH2:15])[CH2:10][CH2:9]1)=O)(C)(C)C.[F:17][C:18]([F:23])([F:22])[C:19]([OH:21])=[O:20]>C(Cl)(Cl)Cl>[F:17][C:18]([F:23])([F:22])[C:19]([OH:21])=[O:20].[C:14]([C:11]1[CH2:12][CH2:13][NH:8][CH2:9][CH:10]=1)(=[O:16])[NH2:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 22482730tert-Butyl 4-carbamoyl-3,6-dihydropyridine-1(2H)-carboxylate

생성물 1

HCID 224827414-Carbamoyl-1,2,3,6-tetrahydropyridine trifluoroacetate

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

In 20 ml of chloroform, 3.7 g of 1-tert-butoxycarbonyl-4-carbamoyl-1,2,3,6-tetrahydropyridine was dissolved, and 13 ml of trifluoroacetic acid were added thereto. The reaction mixture was stirred for 1 hour at room temperature, and subsequently was concentrated under reduced pressure to yield 4.1 g of crude 4-carbamoyl-1,2,3,6-tetrahydropyridine trifluoroacetate as a crystal.

후처리

  1. concentrationsubsequently was concentrated under reduced pressure

출처 및 근거

ORD 기록
ord-bd0780fbc93845618b6d61e206a105ac
출처 데이터셋
uspto-grants-2005_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06894168B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트