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Formamide → 1-(2-Hydroxy-2-phenylethyl)-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one

HRID 732934
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HRID 732934 반응식
[NH2:1][C:2]1[N:6]([CH2:7][CH:8]([OH:15])[C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[N:5]=[CH:4][C:3]=1[C:16]([OH:18])=O.[CH:19]([NH2:21])=O>O>[OH:15][CH:8]([C:9]1[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=1)[CH2:7][N:6]1[C:2]2[N:1]=[CH:19][NH:21][C:16](=[O:18])[C:3]=2[CH:4]=[N:5]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 713FormamideHCID 108794365-amino-1-(2-hydroxy-2-phenylethyl)-1H-pyrazole-4-carboxylic acid

생성물 1

HCID 1363835291-(2-Hydroxy-2-phenylethyl)-1,5-dihydro-4H-pyrazolo[3,4-d]pyrimidin-4-one수율 70%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
190 °C

실험 절차

A suspension of 5 (2.75 g, 10 mmol) in formamide (10 g, 333 mmol) was heated at 190° C. for 8 h and then poured in H2O (300 mL). The crude was filtered and purified by dissolving in 2M NaOH (100 mL), boiling with coal, followed by precipitation with glacial acetic acid. The solid was filtered and recrystallized from absolute ethanol to give 10 (1.79 g, 70%) as a white solid: mp 270-271° C. 1H NMR: δ 4.25-4.55 (m, 2H, CH2), 5.05-5.15 (m, 1H, CHO), 5.65 (d, 1H, OH, disappears with D2O), 7.25-7.45 (m, 5H Ar), 8.05 (s, 1H, H-3), 8.10 (s, 1H, H-6), 12.15 (br s, 1H, NH, disappears with D2O). IR cm−1: 3400 (NH), 3245-2500 (OH), 1740 (CO). Anal. (C13H12N4O2) C, H, N.

후처리

  1. filtrationThe crude was filtered
  2. custompurified
  3. dissolutionby dissolving in 2M NaOH (100 mL)
  4. customfollowed by precipitation with glacial acetic acid
  5. filtrationThe solid was filtered
  6. customrecrystallized from absolute ethanol

출처 및 근거

ORD 기록
ord-86dba6ebcb86496495c52b03710c2216
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07589086B2

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