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

HCID 67168853, 화합물 → Methyl 2-((3S,4S)-4-(aminomethyl)-1-methylpyrrolidin-3-yl)-6-(trifluoromethoxy)benzoate

HRID 716005
노트
인쇄 미리보기

반응식

HRID 716005 반응식
[C:1]([C@H:3]1[CH2:7][N:6]([CH3:8])[CH2:5][C@@H:4]1[C:9]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][C:20]([F:23])([F:22])[F:21])[C:10]=1[C:11]([O:13][CH3:14])=[O:12])#[N:2].C(N1C[C@@H](C#N)[C@H](C2C=CC(Cl)=CC=2C(OC)=O)C1)C1C=CC=CC=1>>[NH2:2][CH2:1][C@H:3]1[CH2:7][N:6]([CH3:8])[CH2:5][C@@H:4]1[C:9]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][C:20]([F:23])([F:21])[F:22])[C:10]=1[C:11]([O:13][CH3:14])=[O:12]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 67168853HCID 67168853, 화합물HCID 131731904HCID 131731904, 화합물

생성물 1

HCID 67168219Methyl 2-((3S,4S)-4-(aminomethyl)-1-methylpyrrolidin-3-yl)-6-(trifluoromethoxy)benzoate

실험 절차

The title compound was prepared according to the procedure outlined in Example 45C substituting the product obtained from Example 110A for the product obtained from Example 45B. In this instance, the aminoester did not cyclize. 1H NMR (300 MHz, DMSO-d6) δ ppm 1.42 (s, 1H) 2.10-2.21 (m, 1H) 2.32-2.48 (m, 4H) 2.55-2.63 (m, 1H) 2.73 (t, J=8.48 Hz, 1H) 2.79-2.87 (m, 3H) 3.87 (s, 3H) 7.28-7.36 (m, 1H) 7.55-7.64 (m, 3H); MS (DCI+) m/z 333.2 [M+H]+.

출처 및 근거

ORD 기록
ord-ba575a08e4ed4628981098fe63ebc031
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09187483B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차출처 및 근거반응 노트