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6-Amino-9-benzyl-2-(2-ethoxyethoxy)-8-methoxypurine → HCID 178467997, 화합물

HRID 2269065
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인쇄 미리보기

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HRID 2269065 반응식
[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][O:14][CH2:15][CH3:16])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([O:24]C)[N:6]2[CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>Cl>[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][O:14][CH2:15][CH3:16])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([OH:24])[N:6]2[CH2:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 183326966-Amino-9-benzyl-2-(2-ethoxyethoxy)-8-methoxypurine

생성물 1

HCID 178467997HCID 178467997, 화합물수율 84%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

6-Amino-9-benzyl-2-(2-ethoxyethoxy)-8-methoxypurine (110 mg, 0.32 mmol) in concentrated hydrochloric acid (20 ml) was stirred at room temperature for 12 hours. The reaction mixture was evaporated in vacuo to dryness and then 28% aqueous ammonia was added thereto. The resulting crystals were filtered to give the subject compound (88 mg, yield 84%).

후처리

  1. customThe reaction mixture was evaporated in vacuo to dryness
  2. addition28% aqueous ammonia was added
  3. filtration
The resulting crystals were filtered

출처 및 근거

ORD 기록
ord-6d7a7f1911c446f5bfbbf3b8857b60ab
출처 데이터셋
uspto-grants-2001_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06329381B1

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