반응 #7739

ord-248d1db259c542e7a6fada3be8fed337

반응 방정식

O=C1CN(C(=O)Cc2ccc(F)cc2)N(C(=O)OCc2ccccc2)C1
2-[2-(4-fluorophenyl)acetyl]-4-oxo-pyrazolidine-1-carboxylic acid benzyl ester
C1COCCN1
morpholine
CC(=O)O[BH-](OC(C)=O)OC(C)=O.[Na+]
Na(OAc)3BH
CC(=O)O
HOAc
Cl
HCl
Cl
HCl
O=C(Cc1ccc(F)cc1)N1CC(N2CCOCC2)CN1C(=O)OCc1ccccc1
desired product
수율 60.0%
O=C(Cc1ccc(F)cc1)N1CC(N2CCOCC2)CN1C(=O)OCc1ccccc1
2-[2-(4-fluorophenyl)acetyl]-4-morpholin-4-yl-pyrazolidine-1-carboxylic acid benzyl ester
수율 60.0%

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타then partitioned between diethyl ether and NaHCO3
  2. 2
    추출The aqueous layer was extracted several times with ether
  3. 3
    기타dried
  4. 4
    농축concentrated in vacuo to a clear oil which
  5. 5
    workup.DISSOLUTIONwas re-dissolved in ether
  6. 6
    여과The solid is collected by filtration

실험 절차

To a solution of 2-[2-(4-fluorophenyl)acetyl]-4-oxo-pyrazolidine-1-carboxylic acid benzyl ester, 11, (0.14 g, 0.4 mmol) and morpholine (0.038 mL, 0.43 mmol) in THF at room temperature is added Na(OAc)3BH (0.125 g, 0.6 mmol) and HOAc (0.022 mL, 0.4 mmol). The solution is stirred 12 hours then partitioned between diethyl ether and NaHCO3. The aqueous layer was extracted several times with ether and the organic layers combined, dried, and concentrated in vacuo to a clear oil which was re-dissolved in ether and one equivalent of ethereal HCl is added and a white solid forms. The solid is collected by filtration and 100 mg (60% yield) of the desired product is isolated as the HCl salt.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07087615B2uspto-grants-2006_08