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

Nitric Acid → HCID 178486766, 화합물

HRID 1042982
노트
인쇄 미리보기

반응식

HRID 1042982 반응식
[N+:1]([O-:4])(O)=[O:2].[CH3:5][C:6]1[C:10]([C:11]2[CH:20]=[C:19]3[C:14]([C:15]([OH:21])=[CH:16][CH:17]=[N:18]3)=[CH:13][CH:12]=2)=[C:9]([CH3:22])[O:8][N:7]=1.[C:23](O)(=[O:26])CC>>[CH3:5][C:6]1[C:10]([C:11]2[CH:20]=[C:19]3[C:14]([C:15]([OH:21])=[C:16]([N+:1]([O-:4])=[O:2])[CH:17]=[N:18]3)=[CH:13][C:12]=2[O:26][CH3:23])=[C:9]([CH3:22])[O:8][N:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 944Nitric AcidHCID 1032Propionic AcidHCID 178434741HCID 178434741, 화합물2회

생성물 1

HCID 178486766HCID 178486766, 화합물수율 82%

반응 조건

온도
100 °C

실험 절차

Nitric acid (10 ml) was added slowly to a solution of 7-(3,5-dimethyl-4-isoxazolyl)-4-quinolinol (for a preparation see Intermediate 14 (28 g, 104 mmol) in propanoic acid (450 ml) at room temperature, followed by heating the reaction mixture to 100° C. for 1 h. After cooling with an ice bath, the precipitate was filtered off, washed with pentane to give the title compound as a yellow powder (27 g, 82%). [APCI-MS] m/z: 314 [M−H]−, Rt 2.12 min. 1H NMR (300 MHz, DMSO-d6, ppm) δ: 13.06 (s, 1H), 9.26 (s, 1H), 7.84 (s, 1H), 7.67 (s, 1H), 3.98 (s, 3H), 2.39 (s, 3H), 2.19 (s, 3H).

후처리

  1. customat room temperature
  2. temperatureAfter cooling with an ice bath
  3. filtrationthe precipitate was filtered off
  4. washwashed with pentane

출처 및 근거

ORD 기록
ord-a1a92247eb6d43df871f2f0762d207ce
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08557984B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트