Hydrochloric Acid → Benzyl 2,9-diazaspiro[5.5]undecane-2-carboxylate hydrochloride
反応式
[CH2:1]1[C:6]2([CH2:11][CH2:10][N:9](C(OC(C)(C)C)=O)[CH2:8][CH2:7]2)[CH2:5][N:4]([C:19]([O:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[O:20])[CH2:3][CH2:2]1.O1CCOCC1.[ClH:35]>CC(OC)(C)C>[ClH:35].[CH2:1]1[C:6]2([CH2:11][CH2:10][NH:9][CH2:8][CH2:7]2)[CH2:5][N:4]([C:19]([O:21][CH2:22][C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)=[O:20])[CH2:3][CH2:2]1参加物
実験手順
To a 20 L temperature controlled reactor with jacket set at 0° C., add a solution of O4-benzyl O9-tert-butyl 4,9-diazaspiro[5.5]undecane-4,9-dicarboxylate (2.06 moles; 838.00 g; 95.65% purity) in 1,4-dioxane (19.63 moles; 1.68 L). When the temperature of the solution is 5° C., add hydrogen chloride (4 M in 1,4-dioxane; 10.32 moles; 2.58 L) at such a rate that the temperature does not rise above 20° C. When the addition is complete, warm the solution to room temperature and stir overnight. Concentrate the reaction mixture under reduced pressure to give a thick slurry. Add MTBE (3.35 L) and agitate the mixture for 30 minutes at 40° C. Allow the mixture to cool to room temperature and filter the precipitate. Wash the precipitate with MTBE (838 mL). Allow the precipitate to dry on the filter and then transfer to a vacuum oven for further drying to give the title compound (638 g; 95% yield) mass spectrum (m/z):289 [M(freebase)+1].
後処理
- customset at 0° C.
- customis 5° C.
- customdoes not rise above 20° C
- additionWhen the addition
- concentrationConcentrate the reaction mixture under reduced pressure
- customto give a thick slurry
- temperatureAllow the mixture to cool to room temperature
- filtrationfilter the precipitate
- washWash the precipitate with MTBE (838 mL)
- customto dry on the
- filtrationfilter
- customfor further drying
出典と根拠
- ORDレコード
- ord-184db9b30fbf40da942e0e498a63d2ec
- 出典データセット
- uspto-grants-2015_09
- 特許番号
- US09145437B2
反応ノート
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