반응 #44788

반응 방정식

NaOH

4-[4-(2-oxazolyl)phenoxy]benzaldehyde

methyl 4-[[(1S,4S)-2,5-diazabicyclo[2.2.1]hept-2-yl]methyl]benzoate

sodium triacetoxyborohydride

→

methyl 4-[[(1S,4S)-5-[[4-[4-(2-oxazolyl)phenoxy]phenyl]methyl]-2,5-diazabicyclo[2.2.1]hept-2-yl]methyl]benzoate

수율 100.0%

용매

dichloroethane

반응 조건

후처리

1. 1
   기타The reaction mixture was separated
2. 2
   추출the aqueous layer was extracted with CH2Cl2
3. 3
   세척The combined organic layers were washed with 0.5 M H2SO4, and MeOH
4. 4
   workup.ADDITIONwas added to the mixture until the precipitated gummy solid
5. 5
   workup.DISSOLUTIONdissolved
6. 6
   기타The layers were separated
7. 7
   온도the aqueous layer was cooled to −5 C
8. 8
   workup.ADDITIONand saturated K2CO3 was added slowly enough
9. 9
   기타ester hydrolysis
10. 10
    추출Once the pH was 11, the solution was extracted with EtOAc (2×)
11. 11
    건조the combined EtOAc fractions were dried
12. 12
    농축concentrated

실험 절차

4-[4-(2-oxazolyl)phenoxy]benzaldehyde (10.2 g, 38.5 mmol) and methyl 4-[[(1S,4S)-2,5-diazabicyclo[2.2.1]hept-2-yl]methyl]benzoate (9.9 g, 40.4 mmol, 1.05 equiv.) were dissolved in dichloroethane (200 mL). After 75 minutes, sodium triacetoxyborohydride (9.8 g, 46.1 mmol, 1.2 equiv.) was added. The reaction mixture was stirred overnight at ambient temperature. Then, 1N NaOH was added. The reaction mixture was separated and the aqueous layer was extracted with CH2Cl2. The combined organic layers were washed with 0.5 M H2SO4, and MeOH was added to the mixture until the precipitated gummy solid dissolved. The layers were separated and the aqueous layer was cooled to −5 C. and saturated K2CO3 was added slowly enough to keep the temperature below 0 C. to prevent ester hydrolysis. Once the pH was 11, the solution was extracted with EtOAc (2×), and the combined EtOAc fractions were dried and concentrated to give 19.0 g (100%) of methyl 4-[[(1S,4S)-5-[[4-[4-(2-oxazolyl)phenoxy]phenyl]methyl]-2,5-diazabicyclo[2.2.1]hept-2-yl]methyl]benzoate as the free base, which was 98% pure by HPLC; 1H NMR (300 MHz, CDCl3) δ 8.02 (d, 2H), 8.02 (d, 2H), 7.69 (d, 1H), 7.47 (d, 2H), 7.40 (d, 2H), 7.22 (d, 1H), 7.08 (d, 2H), 7.05 (d, 2H), 3.92 (s, 3H), 3.84 (d, 1H), 3.78 (d, 1H), 3.77 (d, 1H), 3.71 (d, 1H), 3.35 (s, 1H), 3.31 (s, 1H), 2.89 (d, 1H), 2.88 (d, 1H), 2.71 (dd, 1H), 2.70 (dd, 1H), 1.79 (s, 2H) ppm.

출처