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p-Toluenesulfonic acid → 6-Chloro-9-isopropyl-9H-purine

HRID 1518331
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인쇄 미리보기

반응식

HRID 1518331 반응식
[Cl:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]([NH:8][CH:9]([CH3:11])[CH3:10])[C:3]=1[NH2:12].[CH:13](OCC)(OCC)OCC.C1(C)C=CC(S(O)(=O)=O)=CC=1>>[Cl:1][C:2]1[N:7]=[CH:6][N:5]=[C:4]2[C:3]=1[N:12]=[CH:13][N:8]2[CH:9]([CH3:10])[CH3:11]
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참가 물질

4

반응물 3

HCID 6101p-Toluenesulfonic acidHCID 31214Ethyl orthoformateHCID 71471626-Chloro-N4-isopropylpyrimidine-4,5-diamine

생성물 1

HCID 4146346-Chloro-9-isopropyl-9H-purine

반응 조건

온도
115 °C

실험 절차

Compound 52A (268 mg, 1.44 mmol), triethyl orthoformate (2.4 ml, 14.36 mmol) and para-toluenesulfonic acid (27.3 mg, 0.144 mmol) were combined and heated at 115° C. overnight. Precipitation occurred upon cooling to room temperature. The precipitate was collected via filtration, rinsed with diethyl ether and dried under reduced pressure to yield the title compound 52B: 1H NMR (300 MHz, DMSO-d6) δ ppm 8.81 (1H, s), 8.78 (1H, s), 4.89 (1H, m), 1.58 (6H, d).

후처리

  1. customPrecipitation
  2. temperatureupon cooling to room temperature
  3. filtrationThe precipitate was collected via filtration
  4. washrinsed with diethyl ether
  5. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-d25d24ee366342508d893b1681f020ec
출처 데이터셋
uspto-grants-2012_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08232273B2

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