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3-(Dimethylamino)-2-propenal → 3-Tert-butylpyrazolo[1,5-a]pyrimidin-2-amine

HRID 1912908
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인쇄 미리보기

반응식

HRID 1912908 반응식
[C:1]([C:5]1[C:6]([NH2:11])=[N:7][NH:8][C:9]=1[NH2:10])([CH3:4])([CH3:3])[CH3:2].CN(C)[CH:14]=[CH:15][CH:16]=O>C(O)C.C(O)(=O)C>[C:1]([C:5]1[C:6]([NH2:11])=[N:7][N:8]2[CH:16]=[CH:15][CH:14]=[N:10][C:9]=12)([CH3:4])([CH3:2])[CH3:3]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 791253-(Dimethylamino)-2-propenalHCID 68753336HCID 68753336, 화합물

생성물 1

HCID 687554713-Tert-butylpyrazolo[1,5-a]pyrimidin-2-amine수율 72.8%

시약·촉매·용매 2

HCID 176Acetic Acid촉매HCID 702Ethanol용매

실험 절차

A mixture from Example 105A (2.61 g, 16.9 mmol), 3-dimethylaminoacrylaldehyde (2.0 mL, 20.0 mmol) and acetic acid (25 μL, 0.44 mmol) in ethanol (18 mL) was heated by microwave to 150° C. for 30 minutes. The mixture was cooled to ambient temperature and concentrated. Purification by silica gel chromatography (EtOAc, Rf=0.39) afforded 2.34 g (43%) of the title compound. MS (DCI) m/z 191 (M+H)+.

후처리

  1. concentrationconcentrated
  2. customPurification by silica gel chromatography (EtOAc, Rf=0.39)

출처 및 근거

ORD 기록
ord-15598afda19948d0904f9d8635cab8ee
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08609669B2

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