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Sodium Hydroxide → 2-Amino-3-benzyl-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one

HRID 1805856
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인쇄 미리보기

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HRID 1805856 반응식
[CH2:1]([N:8]1[C:13](=[O:14])[C:12]2[NH:15][CH:16]=[CH:17][C:11]=2[N:10]=[C:9]1/[N:18]=C/N(C)C)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>CO>[NH2:18][C:9]1[N:8]([CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[C:13](=[O:14])[C:12]2[NH:15][CH:16]=[CH:17][C:11]=2[N:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 57693601N'-(3-benzyl-4-oxo-5H-pyrrolo[3,2-d]pyrimidin-2-yl)-N,N-dimethylmethanimidamide

생성물 1

HCID 153761052-Amino-3-benzyl-3H-pyrrolo[3,2-d]pyrimidin-4(5H)-one

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
100 °C

실험 절차

To a mixture of (E)-N′-(3-benzyl-4-oxo-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-2-yl)-N,N-dimethylformimidamide (21.2 g, 0.07 mol) in MeOH (382 mL) was added 3M NaOH (276 mL) and heated at 100° C. for 5 h. After completion of the reaction, the reaction mixture was cooled to 0° C. The solid was filtered (15.8 g, 91%) and used in the next step without further purification.

후처리

  1. customAfter completion of the reaction
  2. temperaturethe reaction mixture was cooled to 0° C
  3. filtrationThe solid was filtered (15.8 g, 91%)
  4. customused in the next step without further purification

출처 및 근거

ORD 기록
ord-99f440b2c938406bb8aebd5d42b131c8
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08354532B2

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