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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 13406007, 화합물 → HCID 178522251, 화합물

HRID 1179669
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HRID 1179669 반응식
C[O:2][C:3]1[N:8]=[CH:7][C:6]([NH:9][C:10](=[O:17])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:5][CH:4]=1>O1CCCC1>[OH:2][C:3]1[N:8]=[CH:7][C:6]([NH:9][C:10](=[O:17])[C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:5][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 13406007HCID 13406007, 화합물

생성물 1

HCID 178522251HCID 178522251, 화합물수율 53.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

반응 조건

온도
180 °C

실험 절차

N-(6-Methoxy-pyridin-3-yl)-benzamide (2.38 g, 10.4 mmol) was dissolved in a mixture of tetrahydrofuran and diethyl ether. HCl-gas was bubbled into the solution for 5 minutes. More diethyl ether was added and the white precipitate was collected by suction, washed twice with diethyl ether and heated in a kugelrohr apparatus at 180° C. for 0.5 hours. The solid material was crystallised from methanol:water, washed twice with water and dried overnight in a vacuum oven, yielding the title compound (1.19 g, 53% yield) as a grey solid.

후처리

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
  1. customwas bubbled into the solution for 5 minutes
  2. additionMore diethyl ether was added
  3. customthe white precipitate was collected by suction
  4. washwashed twice with diethyl ether
  5. customThe solid material was crystallised from methanol
  6. washwater, washed twice with water
  7. customdried overnight in a vacuum oven

출처 및 근거

ORD 기록
ord-cb9e1f5115654c5e985365b4ba63b061
출처 데이터셋
uspto-grants-2007_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07279470B2

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