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tert-Butylhydrazine monohydrochloride → 1-Tert-butoxycarbonyl-4-(1-tert-butyl-3-methyl-5-pyrazolyl)piperazine

HRID 1791927
ノート
印刷プレビュー

反応式

HRID 1791927 の反応式
[C:1]([N:7]1[CH2:12][CH2:11][N:10]([C:13]([O:15][C:16]([CH3:19])([CH3:18])[CH3:17])=[O:14])[CH2:9][CH2:8]1)(=O)[CH2:2][C:3]([CH3:5])=O.Cl.Cl.Cl.CC1C=C(N2CCN([C@@H]3CN[C@H](C(N4CCSC4)=O)C3)CC2)N(C2C=CC=CC=2)N=1.Cl.[C:54]([NH:58][NH2:59])([CH3:57])([CH3:56])[CH3:55]>C(O)C>[C:16]([O:15][C:13]([N:10]1[CH2:11][CH2:12][N:7]([C:1]2[N:58]([C:54]([CH3:57])([CH3:56])[CH3:55])[N:59]=[C:3]([CH3:5])[CH:2]=2)[CH2:8][CH2:9]1)=[O:14])([CH3:19])([CH3:18])[CH3:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 81889tert-Butylhydrazine monohydrochlorideHCID 22028659HCID 22028659、化合物HCID 67507852HCID 67507852、化合物

生成物 1

HCID 220289911-Tert-butoxycarbonyl-4-(1-tert-butyl-3-methyl-5-pyrazolyl)piperazine収率 18.9%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

1-Acetoacetyl-4-tert-butoxycarbonylpiperazine [product of Example 222 (1), 3.92 g] was dissolved in ethanol (300 mL), and tert-butylhydrazine hydrochloride (1.81 g) and molecular sieves 3A (10 g) were added thereto at room temperature. The mixture was stirred for 15 hr. The reaction mixture was filtrated and the filtrate was concentrated under reduced pressure. The residue was dissolved in pyridine (200 mL), and phosphorus oxychloride (3.0 mL) was added thereto at room temperature. The mixture was stirred for 24 hr. The reaction mixture was concentrated under reduced pressure, the residue was acidified with dilute hydrochloric acid to pH 3. The mixture was extracted with ethyl acetate. The extract was washed successively with saturated aqueous sodium hydrogencarbonate solution and brine and dried. The solvent was evaporated under reduced pressure and the residue was purified by silica gel chromatography to give 1-tert-butoxycarbonyl-4-(1-tert-butyl-3-methyl-5-pyrazolyl)piperazine (886 mg) as an oil.

後処理

  1. customat room temperature
  2. filtrationThe reaction mixture was filtrated
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. dissolutionThe residue was dissolved in pyridine (200 mL)
  5. additionphosphorus oxychloride (3.0 mL) was added
  6. customat room temperature
  7. stirringThe mixture was stirred for 24 hr
  8. concentrationThe reaction mixture was concentrated under reduced pressure
  9. extractionThe mixture was extracted with ethyl acetate
  10. washThe extract was washed successively with saturated aqueous sodium hydrogencarbonate solution and brine
  11. customdried
  12. customThe solvent was evaporated under reduced pressure
  13. customthe residue was purified by silica gel chromatography

出典と根拠

ORDレコード
ord-fff3605f9f014a9eafe9279be4b48ca9
出典データセット
uspto-grants-2006_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07074794B2

反応ノート

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