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

HRID 1006589
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HRID 1006589 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
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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. addition(4.1 ml, 29.1 mmol) were added
  2. temperaturethen cooled
  3. filtrationFiltered off product
  4. washwashed precipitate with 100 ml 1M HCl and 200 ml water
  5. customThe solid was dried in vacuum over overnight at 70° C.

출처 및 근거

ORD 기록
ord-7976a1cee66449229a5f356cd665557b
출처 데이터셋
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06790958B2

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