反应 #657280

ord-6e59bf793ede439baead50cdd65e7e53

反应方程式

CON1CCC2(CC1)C(OCc1ccccc1)=C(c1c(C)cc(C)cc1C)C(=O)N2CC1CC1
4-benzyloxy-1-cyclopropylmethyl-8-methoxy-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one
CON1CCC2(CC1)C(O)=C(c1c(C)cc(C)cc1C)C(=O)N2CC1CC1
1-cyclopropylmethyl-4-hydroxy-8-methoxy-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他a temperature of 35° C.
  2. 2
    浓缩The collected product solution was concentrated
  3. 3
    其他the residue purified by chromatography on silica gel (ethyl acetate/heptane 1:1)

实验过程

Debenzylation was conducted using an H-Cube® continuous-flow hydrogenator: 4-benzyloxy-1-cyclopropylmethyl-8-methoxy-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one (546 mg, 1.34 mmol) was dissolved in methanol (47 ml) and this substrate solution (0.029 M) pumped twice through a 5% Pd/C filled cartridge at a flow-rate of 1 mL/min, a temperature of 35° C. and a pressure of 2-3 bars. The collected product solution was concentrated, and the residue purified by chromatography on silica gel (ethyl acetate/heptane 1:1). Yield: 215 mg of 1-cyclopropylmethyl-4-hydroxy-8-methoxy-3-(2,4,6-trimethyl-phenyl)-1,8-diaza-spiro[4.5]dec-3-en-2-one (title compound P2.8) as a white solid, mp 223-225° C.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09023760B2uspto-grants-2015_05