반응 #56793

반응 방정식

ethyl 4-bromobutyrate

compound 8b

3-[2(R)-amino-2-(isobutyl)ethyl]-5-(2-chloro-3-methoxyphenyl)-1-[2-fluoro-6-(trifluoromethyl)benzyl]pyrimidine-2,4 (1H,3H)-dione

K2CO3

→

compound 8c

3-[2(R)-{ethoxycarbonylpropyl-amino}-2-(isobutyl)ethyl]-5-(2-chloro-3-methoxyphenyl)-1-[2-fluoro-6-(trifluoromethyl)benzyl]pyrimidine-2,4(1H,3H)-dione

용매

DMF

반응 조건

후처리

1. 1
   온도cooled to room temperature
2. 2
   기타partitioned between ethyl acetate and H2O
3. 3
   세척The organic layer was washed with brine
4. 4
   건조dried over Na2SO4
5. 5
   농축concentrated
6. 6
   기타The residue was purified by column chromatography on silica gel with ethyl acetate/hexanes/triethylamine 500/500/5

실험 절차

To a solution of compound 8b (25 mg, 0.048 mmol) in DMF (1 mL) was added K2CO3 (21 mg, 0.15 mmol) followed by ethyl 4-bromobutyrate (0.015 mL, 0.1 mmol). The mixture was heated at 95° C. for 16 hours, cooled to room temperature, and partitioned between ethyl acetate and H2O. The organic layer was washed with brine, dried over Na2SO4 and concentrated. The residue was purified by column chromatography on silica gel with ethyl acetate/hexanes/triethylamine 500/500/5 to afford compound 8c . MS (CI) m/z 642.2, 644.2 (MH+).

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