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3-Allylsalicylaldehyde → 6-[4-(3-Allyl-2-hydroxy-benzyl)-piperazin-1-yl]-3H-pyrimidin-4-one

HRID 1993443
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반응식

HRID 1993443 반응식
[N:1]1([C:7]2[N:12]=[CH:11][NH:10][C:9](=[O:13])[CH:8]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[CH2:14]([C:17]1[CH:24]=[CH:23][CH:22]=[C:19]([CH:20]=O)[C:18]=1[OH:25])[CH:15]=[CH2:16]>>[CH2:14]([C:17]1[C:18]([OH:25])=[C:19]([CH:22]=[CH:23][CH:24]=1)[CH2:20][N:4]1[CH2:5][CH2:6][N:1]([C:7]2[N:12]=[CH:11][NH:10][C:9](=[O:13])[CH:8]=2)[CH2:2][CH2:3]1)[CH:15]=[CH2:16]
참가 물질실험 절차출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 1410623-AllylsalicylaldehydeHCID 1361025406-piperazin-1-yl-3H-pyrimidin-4-one2회

생성물 1

HCID 1361025496-[4-(3-Allyl-2-hydroxy-benzyl)-piperazin-1-yl]-3H-pyrimidin-4-one

실험 절차

6-[4-(3-Allyl-2-hydroxy-benzyl)-piperazin-1-yl]-3H -pyrimidin-4-one was prepared using Procedure B from 6-piperazin-1-yl-3H-pyrimidin-4-one (Intermediate 4) and 3-allylsalicylaldehyde (available from Aldrich). 1H NMR (400 MHz, CDCl3) δ 2.58-2.64 (m, 4H), 3.38 (s, 2H), 3.58-3.63 (m, 4H), 3.89 (s, 2H), 5.06-5.15 (m, 2H), 5.39 (s, 1H), 5.97-6.06 (m, 1H), 6.73-6.77 (m, 1H), 6.85-6.89 (m, 1H), 6.99-7.08 (m, 1H), 7.84 (s, 1H), 10.65 (br s, 1H), 12.31 (br s, 1H). Mass spectrum (ES) MH+=327.

출처 및 근거

ORD 기록
ord-12ccd7d9076c46e3a728e039fea643d7
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07652013B2

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