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Formamidine acetate → 6-(furan-2-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-ol

HRID 1786931
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반응식

HRID 1786931 반응식
[NH2:1][C:2]1[CH:6]=[C:5]([C:7]2[O:8][CH:9]=[CH:10][CH:11]=2)[NH:4][C:3]=1[C:12]([O:14]CC)=O.C(O)(=O)C.[CH:21](N)=[NH:22]>C(O)C>[O:8]1[CH:9]=[CH:10][CH:11]=[C:7]1[C:5]1[NH:4][C:3]2[C:12](=[O:14])[NH:22][CH:21]=[N:1][C:2]=2[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 160693Formamidine acetateHCID 10751393ethyl 3-amino-5-(furan-2-yl)-1H-pyrrole-2-carboxylate

생성물 1

HCID 1357417756-(furan-2-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-ol수율 95.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a solution of ethyl 3-amino-5-(2-furyl)-1H-pyrrole-2-carboxylate (2.58 g) in ethanol (35 mL) was added formamidine acetate (1.83 g), and the mixture was heated under reflux for 18 hrs. After cooling to room temperature, the precipitated solid was collected by filtration, washed with ethanol, and dried under reduced pressure at 60° C. to give the title compound (2.26 g).

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 18 hrs
  3. filtrationthe precipitated solid was collected by filtration
  4. washwashed with ethanol
  5. customdried under reduced pressure at 60° C.

출처 및 근거

ORD 기록
ord-95a54f43fb5e4d08b1d87ebe133e79b5
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07507740B2

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