반응 #657282

ord-eaf3c967664f47a08ffe7fc1850bf98a

반응 방정식

Cl
HCl
[Cl-].[NH4+]
ammonium chloride
COC(=O)C1(N(C)C(=O)Cc2c(C)cc(C)cc2C)CCN(OC)CC1
1-methoxy-4-{methyl-[2-(2,4,6-trimethyl-phenyl)-acetyl]-amino}-piperidine-4-carboxylic acid methyl ester
C[O-].[Na+]
sodium methoxide
CON1CCC2(CC1)C(O)=C(c1c(C)cc(C)cc1C)C(=O)N2C
4-hydroxy-8-methoxy-1-methyl-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITat room temperature for 1 hour
  2. 2
    추출thoroughly extracted with ethyl acetate
  3. 3
    세척The combined organic layers were washed with water and brine
  4. 4
    건조dried over sodium sulfate
  5. 5
    농축concentrated
  6. 6
    기타the residue dried in vacuo

실험 절차

To a solution of 1-methoxy-4-{methyl-[2-(2,4,6-trimethyl-phenyl)-acetyl]-amino}-piperidine-4-carboxylic acid methyl ester (85.0 g, 234.5 mmol) in dimethylformamide (800 ml) at 0° C. was added sodium methoxide (38.0 g, 703.5 mmol) in four portions and stirring continued at 0° C. for 30 minutes, then at room temperature for 1 hour. The reaction mixture was poured on ice and saturated aqueous ammonium chloride, acidified to pH 5-6 with concentrated HCl and thoroughly extracted with ethyl acetate. The combined organic layers were washed with water and brine, dried over sodium sulfate, concentrated and the residue dried in vacuo. Yield: 72.7 g of 4-hydroxy-8-methoxy-1-methyl-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one (title compound P2.2) as a solid.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09023760B2uspto-grants-2015_05