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

1-Ethynyl-4-fluorobenzene → 2-(4-Fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine

HRID 1890256
노트
인쇄 미리보기

반응식

HRID 1890256 반응식
[N:1]1O[C:3]([O-])=[C:4]2[CH2:9][CH2:8][CH2:7][CH2:6][N+:5]=12.[F:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]#C)=[CH:14][CH:13]=1>C1(C)C=C(C)C=C(C)C=1>[F:11][C:12]1[CH:17]=[CH:16][C:15]([C:18]2[CH:3]=[C:4]3[CH2:9][CH2:8][CH2:7][CH2:6][N:5]3[N:1]=2)=[CH:14][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 5226271-Ethynyl-4-fluorobenzeneHCID 118450904,5,6,7-Tetrahydro-(1,2,3)oxadiazolo(3,4-a)pyridin-8-ium-3-olate

생성물 1

HCID 674383212-(4-Fluorophenyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyridine수율 27%

시약·촉매·용매 1

HCID 7947Mesitylene용매

반응 조건

온도
165 °C

실험 절차

A mixture of 2.44 g (16.5 mmol) of 4,5,6,7-tetrahydro[1,2,3]oxadiazolo[3,4-a]pyridin-8-ium 3-olate and 2.15 g (16.5 mmol) of 4-fluorophenylacetylene in 80 ml of mesitylene is stirred under argon at 165° C. for 16 h. After cooling, the reaction mixture is concentrated under reduced pressure. Purification by column chromatography on silica gel (cyclohexane/ethyl acetate) gives 888 mg (27%) of the desired product; log P(HCOOH): 2.76; 1H-NMR (MeCN-d3): 7.76 (dd, 2H), 7.11 (dd, 2H), 6.29 (s, 1H), 4.09 (dd, 2H), 2.79 (dd, 2H), 2.02 (m, 2H), 1.84 (m, 2H).

후처리

  1. temperatureAfter cooling
  2. concentrationthe reaction mixture is concentrated under reduced pressure
  3. customPurification by column chromatography on silica gel (cyclohexane/ethyl acetate)

출처 및 근거

ORD 기록
ord-caf551ea99aa4aeb8f6b04a51bf1494b
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507472B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트