반응 #941087

반응 방정식

3′,3′-dimethyl-3′,4′-dihydro-2′H-spiro[1,3-dioxane-2,10′-pyrimido[1,2-a]indole]-8′-carboxylic acid

(2S)-2-(phenoxymethyl)pyrrolidine

DCC

HOBT

Et3N

→

title compound

수율 20.0%

3,3-Dimethyl-8-{[(2S)-2-(phenoxymethyl)pyrrolidin-1-yl]carbonyl}-3,4-dihydropyrimido[1,2-a]indol-10(2H)-one

수율 20.0%

용매

CH2Cl2

반응 조건

후처리

1. 1
   여과The reaction was filtered through 1 cm of silica gel washing with EtOAc
2. 2
   건조The filtrate was dried over Na2SO4
3. 3
   여과filtered
4. 4
   농축concentrated
5. 5
   기타purified on silica gel eluting with acetone/hexane (30/70)
6. 6
   workup.DISSOLUTIONThe resulting white foam was dissolved in CH2Cl2 (1.5 mL)
7. 7
   workup.ADDITIONmethanesulfonic acid (1 mL) was added
8. 8
   workup.STIRRINGthe solution was stirred at rt overnight
9. 9
   workup.ADDITIONThe reaction was poured onto ice
10. 10
    추출extracted with EtOAc (3×)
11. 11
    건조The combined organic extracts were dried over Na2SO4
12. 12
    여과filtered
13. 13
    농축concentrated
14. 14
    기타purified on Biotage Si 12+M cartridge silica gel eluting with acetone/hexane (35/65)

실험 절차

To a solution of 3′,3′-dimethyl-3′,4′-dihydro-2′H-spiro[1,3-dioxane-2,10′-pyrimido[1,2-a]indole]-8′-carboxylic acid (0.090 g, 0.284 mmol) in CH2Cl2 (7 mL) was added (2S)-2-(phenoxymethyl)pyrrolidine (0.75 g, 0.427 mmol), DCC (0.082 g, 0.039 mmol), HOBT (0.038 g, 0.281 mmol) and Et3N (0.045 mL, 0.277 mmol) and the solution stirred overnight at rt. The reaction was filtered through 1 cm of silica gel washing with EtOAc. The filtrate was dried over Na2SO4, filtered, concentrated and purified on silica gel eluting with acetone/hexane (30/70). The resulting white foam was dissolved in CH2Cl2 (1.5 mL) and methanesulfonic acid (1 mL) was added and the solution was stirred at rt overnight. The reaction was poured onto ice, basified to pH 11 with ammonium hydroxide and extracted with EtOAc (3×). The combined organic extracts were dried over Na2SO4, filtered, concentrated and purified on Biotage Si 12+M cartridge silica gel eluting with acetone/hexane (35/65) to give the title compound as a yellow foam (0.021 g, 20%). NMR (400 Mz, DMSO-d6): consistent. MS (ES+) m/z 418.3 [M+H].

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