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N-Iodosuccinimide → HCID 178432607, 화합물

HRID 536497
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HRID 536497 반응식
[CH3:1][C:2]1[N:7]=[C:6]2[NH:8][N:9]=[CH:10][C:5]2=[CH:4][N:3]=1.[I:11]N1C(=O)CCC1=O>CN(C=O)C>[I:11][C:10]1[C:5]2[C:6](=[N:7][C:2]([CH3:1])=[N:3][CH:4]=2)[NH:8][N:9]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 120273N-IodosuccinimideHCID 221154376-methyl-1H-pyrazolo[3,4-d]pyrimidine

생성물 1

HCID 178432607HCID 178432607, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
80 °C

실험 절차

2.180 g (purity 73%, approx. 11.82 mmol) of 6-methyl-1H-pyrazolo[3,4-d]pyrimidine and 3.987 g (17.72 mmol) of N-iodosuccinimide were dissolved in 30 ml DMF and heated for 2 h at 80° C. After cooling, the mixture was concentrated in the rotary evaporator and the residue was mixed with dichloromethane, filtered with suction and dried under high vacuum. 7.950 g (approx. 38% purity) of the target compound was obtained.

후처리

  1. temperatureAfter cooling
  2. concentrationthe mixture was concentrated in the rotary evaporator
  3. additionthe residue was mixed with dichloromethane
  4. filtrationfiltered with suction
  5. customdried under high vacuum
  6. custom7.950 g (approx. 38% purity) of the target compound was obtained

출처 및 근거

ORD 기록
ord-1d4cadfa36524ffbb0d8d2eee00f7fd3
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859569B2

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