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Hydrochloric Acid → 1-(4-methylphenyl)-3-(propan-2-yl)-1H-pyrazol-5-amine

HRID 2069116
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HRID 2069116 반응식
[C:1](#[N:3])C.[CH3:4][C:5]([O-])([CH2:7][CH3:8])[CH3:6].[K+].C(OCC)(=O)C(C)C.Cl.[C:20]1([CH3:28])[CH:25]=[CH:24][C:23]([NH:26][NH2:27])=[CH:22][CH:21]=1.Cl>C1COCC1.C(O)C>[CH:5]([C:7]1[CH:8]=[C:1]([NH2:3])[N:26]([C:23]2[CH:24]=[CH:25][C:20]([CH3:28])=[CH:21][CH:22]=2)[N:27]=1)([CH3:6])[CH3:4]
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참가 물질

8

반응물 5

HCID 313Hydrochloric AcidHCID 6342AcetonitrileHCID 7342Ethyl isobutyrateHCID 125044-Methylphenylhydrazine monohydrochlorideHCID 23683543Potassium t-amylate

생성물 1

HCID 433814411-(4-methylphenyl)-3-(propan-2-yl)-1H-pyrazol-5-amine수율 86.4%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 8028Tetrahydrofuran용매

실험 절차

To a mixture of acetonitrile (0.50 mL, 9.57 mmol) in THF (30 ml) at RT was added potassium 2-methylbutan-2-olate (1.7M solution in 2-methyl-butan-2-ol, 16.9 mL, 28.7 mmol). On completion of the addition ethyl isobutyrate (5.12 mL, 38.3 mmol) was added dropwise and the mixture was maintained at RT for 16 hr. The reaction mixture was concentrated in vacuo to ca 20 mL, was diluted with ethanol (20 mL) and p-tolylhydrazine hydrochloride (1.52 g, 9.57 mmol) was added. The resulting mixture was acidified to pH1 by the addition of conc. hydrochloric acid and the mixture was then heated to 70° C. for 2 hr. The mixture was cooled to RT and was concentrated in vacuo to ca 20 mL and then diluted with water (30 mL). The aq. mixture was adjusted to pH12 by the addition of aq NaOH solution (6M) and was then extracted with EtOAc (2×20 mL). The combined organic extracts were washed with brine (30 mL) and then dried (MgSO4) and evaporated in vacuo to afford the title compound as a brown oil (1.78 g, 90% pure, 72%); Rt 1.32 min (Method 2); m/z 216 (M+H)+ (ES+). This material was used directly in the next step, without further purification.

후처리

  1. additionwas added dropwise
  2. concentrationThe reaction mixture was concentrated in vacuo to ca 20 mL
  3. additionwas added
  4. temperaturethe mixture was then heated to 70° C. for 2 hr
  5. temperatureThe mixture was cooled to RT
  6. concentrationwas concentrated in vacuo to ca 20 mL
  7. additiondiluted with water (30 mL)
  8. additionThe aq. mixture was adjusted to pH12 by the addition of aq NaOH solution (6M)
  9. extractionwas then extracted with EtOAc (2×20 mL)
  10. washThe combined organic extracts were washed with brine (30 mL)
  11. dry with materialdried (MgSO4)
  12. customevaporated in vacuo

출처 및 근거

ORD 기록
ord-dcb9b07a2d5a4dff9fa39e08563b22ab
출처 데이터셋
uspto-grants-2012_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08299074B2

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