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

Putrescine → 6-[(4-Aminobutyl)amino]-3-pyridinecarbonitrile

HRID 2281965
노트
인쇄 미리보기

반응식

HRID 2281965 반응식
Cl[C:2]1[N:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=1.[NH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH2:15]>>[NH2:10][CH2:11][CH2:12][CH2:13][CH2:14][NH:15][C:2]1[N:7]=[CH:6][C:5]([C:8]#[N:9])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 1045PutrescineHCID 51520946-Chloro-3-pyridinecarbonitrile

생성물 1

HCID 570445896-[(4-Aminobutyl)amino]-3-pyridinecarbonitrile

반응 조건

온도
170 °C

실험 절차

6-Chloro-3-pyridinecarbonitrile (5.0 g) was dissolved in 1,4-diaminobutane (50 ml), and the solution was stirred at 170° C. for 2 hours with heating. Diethyl ether and distilled water were added to the reaction mixture, the layers were separated, and the aqueous layer was extracted with diethyl ether. The aqueous layer was saturated with sodium chloride, and the resulting mixture was extracted with chloroform. The resulting organic layer was dried over anhydrous magnesium sulfate, and filtered, and the filtrate was concentrated under reduced pressure to obtain the title compound (4.77 g).

후처리

  1. temperaturewith heating
  • distillationDiethyl ether and distilled water
  • additionwere added to the reaction mixture
  • customthe layers were separated
  • extractionthe aqueous layer was extracted with diethyl ether
  • extractionthe resulting mixture was extracted with chloroform
  • dry with materialThe resulting organic layer was dried over anhydrous magnesium sulfate
  • filtrationfiltered
  • concentrationthe filtrate was concentrated under reduced pressure
  • 출처 및 근거

    ORD 기록
    ord-d55adc20c14845db9834123deff5324f
    출처 데이터셋
    uspto-grants-2015_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US09139609B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트