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Hydrochloric Acid → N-(1-methyl-1H-pyrazol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-6-amine

HRID 594958
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반응식

HRID 594958 반응식
[CH3:1][N:2]1[CH:6]=[C:5]([NH2:7])[CH:4]=[N:3]1.Cl[C:9]1[N:14]=[C:13]2[NH:15][N:16]=[CH:17][C:12]2=[CH:11][N:10]=1.Cl>C(O)(C)C>[CH3:1][N:2]1[CH:6]=[C:5]([NH:7][C:9]2[N:14]=[C:13]3[NH:15][N:16]=[CH:17][C:12]3=[CH:11][N:10]=2)[CH:4]=[N:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 47709901-methyl-1H-pyrazol-4-amineHCID 529112546-chloro-1H-pyrazolo[3,4-d]pyrimidine

생성물 1

HCID 66765655N-(1-methyl-1H-pyrazol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-6-amine

시약·촉매·용매 1

HCID 3776Isopropanol용매

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온도
140 °C

실험 절차

A suspension of 1-methyl-1H-pyrazol-4-amine (173 mg, 1.29 mmol), 6-chloro-1H-pyrazolo[3,4-d]pyrimidine (200 mg, 1.29 mmol) and HCl (25 μL, 4M in dioxane) in isopropanol (2 mL) was heated in the microwave at 140° C. for 1 h. After cooling to rt, the mixture was filtered and the resulting solid washed with cold isopropanol and diethyl ether to give N-(1-methyl-1H-pyrazol-4-yl)-1H-pyrazolo[3,4-d]pyrimidin-6-amine.

후처리

  1. temperatureAfter cooling to rt
  2. filtrationthe mixture was filtered
  3. washthe resulting solid washed with cold isopropanol and diethyl ether

출처 및 근거

ORD 기록
ord-8115ee6c24534ecb842ba021ead9b8a8
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09242987B2

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