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Hydrazine hydrate (1:1) → HCID 69372494, 화합물

HRID 1926587
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HRID 1926587 반응식
Cl[C:2]1([NH2:20])[N:19]=[CH:18][N:17]=[C:16]2[C:3]1=[N:4][CH2:5][N:6]2[C@@H:7]1[O:15][C@H:12]([CH2:13][OH:14])[C@@H:10]([OH:11])[C@H:8]1[OH:9].O.[NH2:22][NH2:23]>CO>[NH:22]([NH:20][C:2]1[C:3]2[N:4]=[CH:5][N:6]([C:16]=2[N:17]=[CH:18][N:19]=1)[C@@H:7]1[O:15][C@H:12]([CH2:13][OH:14])[C@@H:10]([OH:11])[C@H:8]1[OH:9])[NH2:23]
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참가 물질

4

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 666015536-Chloroadenosine

생성물 1

HCID 69372494HCID 69372494, 화합물

시약·촉매·용매 1

HCID 887Methanol용매2회

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온도
50 °C

실험 절차

A mixture of 6-chloroadenosine (1 g, 3.5 mmol) and hydrazine monohydrate (5 mL) in MeOH (10 mL) was stirred at 50° C. for 1 hr. The reaction mixture was allowed to cool to room temperature and was then concentrated in vacuo to provide a crude residue which was suspended in MeOH and (10 mL) and stirred at room temperature. The solid product that separated out from the suspension was filtered, washed with MeOH and dried in vacuo to provide N6-hydrazinoadenosine (970 mg) which was used without further purification.

후처리

  1. temperatureto cool to room temperature
  2. concentrationwas then concentrated in vacuo
  3. customto provide a crude residue which
  4. stirring(10 mL) and stirred at room temperature
  5. customThe solid product that separated out from the suspension
  6. filtrationwas filtered
  7. washwashed with MeOH
  8. customdried in vacuo

출처 및 근거

ORD 기록
ord-ad99c95493e645d0babd4b127b3a7a88
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08183224B2

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