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Triethylamine → 2-Chloro-6-(4-phenylbenzylamino)purine

HRID 2215656
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HRID 2215656 반응식
[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([NH:6][CH:7]=[N:8]2)=[C:4](Cl)[N:3]=1.[C:12]1([C:18]2[CH:25]=[CH:24][C:21]([CH2:22][NH2:23])=[CH:20][CH:19]=2)[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1.C(N(CC)CC)C>C(O)CCC>[Cl:1][C:2]1[N:10]=[C:9]2[C:5]([NH:6][CH:7]=[N:8]2)=[C:4]([NH:23][CH2:22][C:21]2[CH:24]=[CH:25][C:18]([C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=3)=[CH:19][CH:20]=2)[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 3449894-PhenylbenzylamineHCID 53244122,6-Dichloropurine

생성물 1

HCID 219518382-Chloro-6-(4-phenylbenzylamino)purine

시약·촉매·용매 1

HCID 2631-Butanol용매

반응 조건

온도
120 °C

실험 절차

The 2,6-dichloropurine (5.0 g, 26.45 mmol) was suspended in n-butanol (50 ml) and the 4-phenylbenzylamine (6.61 g, 29.1 mmol) and triethylamine (4.1 ml, 29.1 mmol) were added. The solution was heated at 120° C. overnight then cooled. Filtered off product using excess n-butanol and washed precipitate with 100 ml 1M HCl and 200 ml water. The solid was dried in vacuum over overnight at 70° C. to give the desired product as a pale yellow solid

후처리

  1. temperaturethen cooled
  2. filtrationFiltered off product
  3. washwashed precipitate with 100 ml 1M HCl and 200 ml water
  4. customThe solid was dried in vacuum over overnight at 70° C.

출처 및 근거

ORD 기록
ord-d1da3c80250b492a81c5217cc28dacd6
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07109330B2

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