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

Dichloromethane → 1~2~,2~2~:2~3~,3~2~-Terpyridine

HRID 25862
노트
인쇄 미리보기

반응식

HRID 25862 반응식
Cl.[C:2](Cl)(=O)[C:3]1[CH:8]=[CH:7][CH:6]=[N:5][CH:4]=1.CC[N:13]([CH:17]([CH3:19])C)[CH:14]([CH3:16])C.CO[C:22]1[CH:27]=CC=[C:24]([NH2:28])[CH:23]=1.[CH2:29](Cl)Cl>>[N:13]1[CH:14]=[CH:16][CH:29]=[CH:19][C:17]=1[C:4]1[C:3]([C:2]2[CH:27]=[CH:22][CH:23]=[CH:24][N:28]=2)=[CH:8][CH:7]=[CH:6][N:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6344DichloromethaneHCID 108243-MethoxyanilineHCID 81531DiisopropylethylamineHCID 884383-Pyridinecarbonyl chloride, hydrochloride (1:1)

생성물 1

HCID 149389711~2~,2~2~:2~3~,3~2~-Terpyridine

실험 절차

Nicotinoyl chloride hydrochloride (0.3 g, 1.685 mmol), DIEA (0.65 g, 5.06 mmol, 3.0 eqv), and ortho- or meta-anisidine (0.21 g, 1.68 mmol, 1 eqv) were dissolved in CH2Cl2 and stirred at rt for 48 h. The solution was extracted with 1N HCl solution. The aqueous layer was neutralized with a NaHCO3 solution and extracted with CH2Cl2. The organic extracts were combined, dried (MgSO4), filtered, and concentrated in vacuo to give a white solid.

후처리

  1. extractionThe solution was extracted with 1N HCl solution
  2. extractionextracted with CH2Cl2
  3. dry with materialdried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customto give a white solid

출처 및 근거

ORD 기록
ord-cb847d7ade3d49c2ad756e823e9807e5
출처 데이터셋
uspto-grants-2005_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06858600B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트