Benzoyl chloride → 1-Piperazinecarboxylic acid, 4-benzoyl-, 1,1-diMethylethyl ester

HRID 1013065노트

반응식

HRID 1013065 반응식
[C:1]([N:8]1[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]1)([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[OH-].[Na+].[C:16](Cl)(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>O1CCOCC1.O.[Cl-].[Na+].O>[C:16]([N:11]1[CH2:10][CH2:9][N:8]([C:1]([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2])[CH2:13][CH2:12]1)(=[O:23])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

참가 물질

7

반응물 3

HCID 7412Benzoyl chlorideHCID 14798Sodium HydroxideHCID 143452tert-Butyl piperazine-1-carboxylate

생성물 1

HCID 185197561-Piperazinecarboxylic acid, 4-benzoyl-, 1,1-diMethylethyl ester수율 90%

시약·촉매·용매 3

HCID 962Water용매HCID 312751,4-Dioxane용매2회HCID 57417360Sodium chloride; water용매

실험 절차

To a solution of N-Boc-piperazine (14) (1.00 g, 5.37 mmol) in dioxane (5 mL), a solution of NaOH (0.50 g, 12.9 mmol) in water (5 mL) followed by a solution of benzoyl chloride (0.75 mL, 6.44 mmol) in dioxane (2 mL) under vigorous stirring were added. The reaction mixture was stirred at ambient temperature for 4 hours, diluted with brine (20 mL), and extracted with ethyl acetate (2×25 mL). The organic extract was washed successively with brine (20 mL), saturated NaHCO3 (20 mL), saturated KH2PO4 (20 mL), and dried (Na2SO4). The solvents were evaporated to give the title compound (1.400 g, 90%) which was used in the next step of the synthesis without further purification. 1H NMR (CDCl3, HMDS), δ: 1.41 (s, 9H), 2.86 (t, J=5.0 Hz, 4H); 3.62 (t, J=5.0 Hz, 4H); 7.34 (s, 5H).

후처리

  1. additionwere added
  2. stirringThe reaction mixture was stirred at ambient temperature for 4 hours
  3. extractionextracted with ethyl acetate (2×25 mL)
  4. extractionThe organic extract
  5. washwas washed successively with brine (20 mL), saturated NaHCO3 (20 mL), saturated KH2PO4 (20 mL)
  6. dry with materialdried (Na2SO4)
  7. customThe solvents were evaporated

출처 및 근거

ORD 기록
ord-ed065e2b6a1b4a89a6369d2f5c1fbfd3
출처 데이터셋
uspto-grants-2011_07
특허 번호
US07981895B2

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