Hydrochloric Acid → Methyl 4-Boc-piperazine-2-acetate

HRID 23208

반응식

HRID 23208 반응식
C([N:8]1[CH2:13][CH2:12][N:11](CC2C=CC=CC=2)[CH2:10][CH:9]1[CH2:21][C:22]([O:24][CH3:25])=[O:23])C1C=CC=CC=1.Cl.C([O-])([O-])=O.[K+].[K+].[CH3:33][C:34]([O:37][C:38]([O:40]N=C(C1C=CC=CC=1)C#N)=O)([CH3:36])[CH3:35]>[Pd].CO>[C:38]([N:11]1[CH2:12][CH2:13][NH:8][CH:9]([CH2:21][C:22]([O:24][CH3:25])=[O:23])[CH2:10]1)([O:37][C:34]([CH3:33])([CH3:35])[CH3:36])=[O:40]

참가 물질

7

반응물 4

HCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 938652-(tert-Butoxycarbonyloxyimino)-2-phenylacetonitrileHCID 22710010Methyl 2-(1,4-dibenzylpiperazin-2-yl)acetate

생성물 1

HCID 2756816Methyl 4-Boc-piperazine-2-acetate수율 76.4%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

The 13.7 g (40 mmol) of methyl 1,4-dibenzylpiperazine-2-acetate, 150 mL of MeOH, 50 mL of 1 N HCl (aqueous) and 3 g of 10% Pd/C were combined and hydrogenated with H2 (50 psi) for 24 hours. The reaction was filtered, the filtrate was concentrated in vacuo to remove most of the MeOH, and the residue was made basic with K2CO3 to pH=9-10, and 9.8 g (40 mmol) of BOC-ON was added slowly at 0° C. The reaction was stirred at 0° for 1 hour, allowed to warm up to room temperature, stirred for 2 hours, and extracted with ethyl acetate (2×200 mL). The combined extracts were treated with 50 mL of 10% HCl (aqueous). The aqueous layer was washed with ethyl acetate, basified with K2CO3 and extracted three times with ethyl acetate. The combined organic layers were washed with brine, dried over MgSO4 and concentrated in vacuo to give 7.89 g of methyl 4-Boc-piperazine-2-acetate; 1H NMR (CDCl3) δ 1.4 (s,9), 2.31 (dd,1), 2.37 (dd, 1), 2.55 (b, 1), 2.69-3.02 (m,4), 3.75 (s,3), 3.88 (b, 2).

후처리

  1. filtrationThe reaction was filtered
  2. concentrationthe filtrate was concentrated in vacuo
  3. customto remove most of the MeOH
  4. additionwas added slowly at 0° C
  5. stirringstirred for 2 hours
  6. extractionextracted with ethyl acetate (2×200 mL)
  7. additionThe combined extracts were treated with 50 mL of 10% HCl (aqueous)
  8. washThe aqueous layer was washed with ethyl acetate
  9. extractionextracted three times with ethyl acetate
  10. washThe combined organic layers were washed with brine
  11. dry with materialdried over MgSO4
  12. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-a859f4b242f8477099a02a6606c472aa
출처 데이터셋
uspto-grants-2005_02
특허 번호
US06849739B2

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