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

N-(Aminocarbonyl)-2-furancarboxamide → N-[[[1-Azabicyclo[2.2.2]octan-3-yl]amino]carbonyl]-2-furancarboxamide

HRID 1030481
노트
인쇄 미리보기

반응식

HRID 1030481 반응식
Cl.Cl.[NH2:3][CH:4]1[CH:9]2[CH2:10][CH2:11][N:6]([CH2:7][CH2:8]2)[CH2:5]1.[O:12]1[CH:16]=[CH:15][CH:14]=[C:13]1[C:17]([NH:19][C:20](N)=[O:21])=[O:18].C(N(C(C)C)CC)(C)C.C([O-])(=O)CCC([O-])=O>N1C=CC=CC=1>[N:6]12[CH2:11][CH2:10][CH:9]([CH2:8][CH2:7]1)[CH:4]([NH:3][C:20]([NH:19][C:17]([C:13]1[O:12][CH:16]=[CH:15][CH:14]=1)=[O:18])=[O:21])[CH2:5]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 73100N-(Aminocarbonyl)-2-furancarboxamideHCID 81531DiisopropylethylamineHCID 160419SuccinateHCID 197853Quinuclidine, 3-amino-, dihydrochloride

생성물 1

HCID 15616405N-[[[1-Azabicyclo[2.2.2]octan-3-yl]amino]carbonyl]-2-furancarboxamide

시약·촉매·용매 1

HCID 1049Pyridine
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
용매

실험 절차

The above compound was prepared, following the procedure of Example 14b, from 3-aminoquinuclidine dihydrochloride (1.0 g, 5 mmol), 2-furoylurea (0.77 g, 5 mmol), and diisopropylethylamine (1.3 g, 10 mmol) in pyridine (20 ml). The product (0.58 g) was converted to the 1:1 succinate mp 156°-159° C.

후처리

  1. customThe above compound was prepared

출처 및 근거

ORD 기록
ord-591c9d9339804ae6a93ad0786d9c66e6
출처 데이터셋
uspto-grants-1992_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05106843

반응 노트

불러오는 중…