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2-Chloronicotinic acid → 2-{4-[2-(2-Hydroxy ethoxy)ethyl]piperazin-1-yl}nicotinic acid

HRID 231775
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반응식

HRID 231775 반응식
[OH:1][CH2:2][CH2:3][O:4][CH2:5][CH2:6][N:7]1[CH2:12][CH2:11][NH:10][CH2:9][CH2:8]1.Cl[C:14]1[N:22]=[CH:21][CH:20]=[CH:19][C:15]=1[C:16]([OH:18])=[O:17]>O1CCOCC1>[OH:1][CH2:2][CH2:3][O:4][CH2:5][CH2:6][N:7]1[CH2:12][CH2:11][N:10]([C:14]2[N:22]=[CH:21][CH:20]=[CH:19][C:15]=2[C:16]([OH:18])=[O:17])[CH2:9][CH2:8]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 762582-Chloronicotinic acidHCID 1394361-[2-(2-Hydroxyethoxy)ethyl]piperazine

생성물 1

HCID 200320142-{4-[2-(2-Hydroxy ethoxy)ethyl]piperazin-1-yl}nicotinic acid

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

Grams 5.9 of 1-(2-hydroxyethoxyethyl)piperazine and 2.7 g of 2-chloronicotinic acid in 50 ml dioxane were refluxed for 3 days. The reaction mixture was then cooled and allowed to rest for 2 days, afterwards the solvent was removed and the residue crystallized from absolute ethanol, gave 1.1 g of 2-{4-[2-(2-hydroxy ethoxy)ethyl]piperazin-1-yl}nicotinic acid melting at 172°-174° C.

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
  1. temperatureThe reaction mixture was then cooled
  2. customafterwards the solvent was removed
  3. customthe residue crystallized from absolute ethanol

출처 및 근거

ORD 기록
ord-3a6e8d7cf8b340888fd9d3b28157e5fc
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04849422

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