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Hydrochloric Acid → 5-(3-chloro-4-cyanophenyl)-1H-pyrazole-4-carbonitrile

HRID 872871
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HRID 872871 반응식
[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2[N:14](C3CCCCO3)[N:13]=[CH:12][C:11]=2[C:21]#[N:22])[CH:5]=[CH:6][C:7]=1[C:8]#[N:9].Cl>C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([C:10]2[NH:14][N:13]=[CH:12][C:11]=2[C:21]#[N:22])[CH:5]=[CH:6][C:7]=1[C:8]#[N:9]
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반응물 2

HCID 313Hydrochloric AcidHCID 671727985-(3-chloro-4-cyanophenyl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-4-carbonitrile

생성물 1

HCID 671733195-(3-chloro-4-cyanophenyl)-1H-pyrazole-4-carbonitrile

시약·촉매·용매 1

HCID 702Ethanol용매2회

실험 절차

To a solution containing 5-(3-chloro-4-cyanophenyl)-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazole-4-carbonitrile (2.686 g, 8.59 mmol) dissolved in ethanol (25 ml), 10% HCl solution in ethanol (50 ml) was added and the resulting mixture was stirred overnight. The crude product was extracted with DCM/water. The pH of the aqueous phase was adjusted to 12 by adding 2 M NaOH. The aqueous phase was again extracted with DCM. The combined organic phases were dried with Na2SO4, filtered and evaporated. The product was purified by flash chromatography. 1H-NMR (400 MHz; DMSO-d6): δ 8.00-8.05 (m, 1H), 8.13-8.19 (m, 2H), 8.75 (s, 1H), 14.24 (s, 1H).

후처리

  1. extractionThe crude product was extracted with DCM/water
  2. additionby adding 2 M NaOH
  3. extractionThe aqueous phase was again extracted with DCM
  4. dry with materialThe combined organic phases were dried with Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe product was purified by flash chromatography

출처 및 근거

ORD 기록
ord-36b591eaaa84466abae4f8086218ef64
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08975254B2

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