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Hydrazine → 6-chloro-1H-pyrazolo[3,4-d]pyrimidine

HRID 474376
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HRID 474376 반응식
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5]([CH:9]=O)=[CH:4][N:3]=1.[NH2:11][NH2:12]>C1COCC1>[Cl:1][C:2]1[N:7]=[C:6]2[NH:11][N:12]=[CH:9][C:5]2=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 9321HydrazineHCID 189831682,4-Dichloropyrimidine-5-carbaldehyde

생성물 1

HCID 529112546-chloro-1H-pyrazolo[3,4-d]pyrimidine수율 34%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

A solution of 2,4-dichloropyrimidine-5-carbaldehyde (7.75 g, 43.8 mmol, Preparation #1) in THF (100 mL) was added to a 500 mL round-bottomed flask charged with anhydrous hydrazine (3.0 mL, 96 mmol) in THF (250 mL). The reaction mixture was allowed to stir at ambient temperature for about 1 h after which the reaction mixture was concentrated under reduced pressure. The crude product was suspended in DCM (100 mL) and filtered through a silica gel pad. The silica gel pad was washed with additional DCM (2×20 mL) and the combined organic layers were concentrated under reduced pressure. The crude material was purified by silica gel chromatography eluting with 30% EtOAc in heptane to provide 6-chloro-1H-pyrazolo[3,4-d]pyrimidine (2.3 g, 34%) as a white solid. LC/MS (Table 2, Method a) Rt=1.29 min; MS m/z: 155 (M+H)+.

후처리

  1. concentrationwas concentrated under reduced pressure
  2. filtrationfiltered through a silica gel pad
  3. washThe silica gel pad was washed with additional DCM (2×20 mL)
  4. concentrationthe combined organic layers were concentrated under reduced pressure
  5. customThe crude material was purified by silica gel chromatography
  6. washeluting with 30% EtOAc in heptane

출처 및 근거

ORD 기록
ord-f80e19c58f7b4a2483c22cb1332978eb
출처 데이터셋
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08637529B2

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