반응 #640603

ord-1345c9612dcd45efb79401cc3bce7f0b

반응 방정식

O
water
CCOC(=O)C1=NOC2(N3CCCC3)CCN(C(C)=O)CC12
5-acetyl-7a-pyrrolidin-1-yl-3a,4,5,6,7,7a-hexahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid ethyl ester
O=C(O)C(F)(F)F
trifluoroacetic acid
CCOC(=O)c1noc2c1CN(C(C)=O)CC2
5-acetyl-4,5,6,7-tetrahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid ethyl ester

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도was heated
  2. 2
    온도to reflux for 8 h
  3. 3
    건조the organic phase was dried over MgSO4
  4. 4
    기타the solvent removed under a vacuum
  5. 5
    기타The remaining brown oil was purified by column chromatography (SiO2, EtOAc/EtOH 10:1)

실험 절차

A mixture of 18.0 g (58 mmol) of 5-acetyl-7a-pyrrolidin-1-yl-3a,4,5,6,7,7a-hexahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid ethyl ester (B) in 150 mL of DCM and 6.47 mL (87 mmol) of trifluoroacetic acid was heated to reflux for 8 h. After addition of 100 mL of water, the organic phase was dried over MgSO4 and the solvent removed under a vacuum. The remaining brown oil was purified by column chromatography (SiO2, EtOAc/EtOH 10:1). 12.5 g (90% of theoretical) of the desired product 5-acetyl-4,5,6,7-tetrahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid ethyl ester (C) were obtained in the form of a brown-yellow oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08048879B2uspto-grants-2011_11