反応 #4043393
関連文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-cdccfb4c979d4d21bf60d03055539d31表示可能な構造データがありません
C1CC2CCC1C(=O)N2製品情報
2-azabicyclo[2.2.2]octan-3-one (CAS 3306-69-2) product identity, structure identifiers and related reaction data for chemical intermediate research and sourcing review.
想定用途
専門的研究・工業用途限定
データベース ID 137887
安全上の注意
For professional research and industrial use only. Review the supplier safety data sheet before handling.
合成データ
12 反応 · 12 文献
反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-cdccfb4c979d4d21bf60d03055539d31反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-de712a579b17422aafa814fe39b05bc7反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b5dffaca6dfe416d9048318d898c032b反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b4bd39c0b76642178ac11de9004563a9反応条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-Azabicyclo[2.2.2]octan-3-one (228 mg, 2.3 mmole) is dissolved in a mixture of THF/DMF (5 mL/3 mL) and treated with NaH (60%, 184 mg, 4.6 mmole). The resulting mixture is heated at 60° C. for 0.5 hour before addition of 2-chloro-6,7-dimethoxyquinoxaline (344 mg, 1.5 mmole). After being heated at 80° C. overnight, the reaction mixture is concentrated . The residue is chromatographed on silica gel (50% ethyl acetate/hexane) to give 164 mg (23%) of a yellow solid (m.p. 158-159° C.). the reaction mixture is concentrated The residue is chromatographed on silica gel (50% ethyl acetate/hexane)
ソース ID: ord-c5946580d86643d89c693cc7815d6d15反応条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-Azabicyclo[2.2.2]octan-3-one (228 mg, 2.3 mmole) is dissolved in a mixture of THF/DMF (5 mL/3 mL) and treated with NaH (60%, 184 mg, 4.6 mmole). The resulting mixture is heated at 60° C. for 0.5 hour before addition of 2-chloro-6,7-dimethoxyquinoxaline (344 mg, 1.5 mmole). After being heated at 80° C. overnight, the reaction mixture is concentrated . The residue is chromatographed on silica gel (50% ethyl acetate/hexane) to give 164 mg (23%) of a yellow solid (m.p. 158-159° C.). the reaction mixture is concentrated The residue is chromatographed on silica gel (50% ethyl acetate/hexane)
ソース ID: ord-c5946580d86643d89c693cc7815d6d15反応条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-Azabicyclo[2.2.2]octan-3-one (228 mg, 2.3 mmole) is dissolved in a mixture of THF/DMF (5 mL/3 mL) and treated with NaH (60%, 184 mg, 4.6 mmole). The resulting mixture is heated at 60° C. for 0.5 hour before addition of 2-chloro-6,7-dimethoxyquinoxaline (344 mg, 1.5 mmole). After being heated at 80° C. overnight, the reaction mixture is concentrated. The residue is chromatographed on silica gel (50% ethyl acetate/hexane) to give 164 mg (23%) of a yellow solid (m.p. 158-159° C.). the reaction mixture is concentrated The residue is chromatographed on silica gel (50% ethyl acetate/hexane)
ソース ID: ord-d4f26f37fe4d4f7f8fb7cf472b32084d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-cdccfb4c979d4d21bf60d03055539d31反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-de712a579b17422aafa814fe39b05bc7反応条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-Azabicyclo[2.2.2]octan-3-one (228 mg, 2.3 mmole) is dissolved in a mixture of THF/DMF (5 mL/3 mL) and treated with NaH (60%, 184 mg, 4.6 mmole). The resulting mixture is heated at 60° C. for 0.5 hour before addition of 2-chloro-6,7-dimethoxyquinoxaline (344 mg, 1.5 mmole). After being heated at 80° C. overnight, the reaction mixture is concentrated. The residue is chromatographed on silica gel (50% ethyl acetate/hexane) to give 164 mg (23%) of a yellow solid (m.p. 158-159° C.). the reaction mixture is concentrated The residue is chromatographed on silica gel (50% ethyl acetate/hexane)
ソース ID: ord-d4f26f37fe4d4f7f8fb7cf472b32084d反応条件: temp:0.00; pressure:0.00; stir:
ソース ID: ord-b4bd39c0b76642178ac11de9004563a9反応条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
実験手順: 2-Azabicyclo[2.2.2]octan-3-one (228 mg, 2.3 mmole) is dissolved in a mixture of THF/DMF (5 mL/3 mL) and treated with NaH (60%, 184 mg, 4.6 mmole). The resulting mixture is heated at 60° C. for 0.5 hour before addition of 2-chloro-6,7-dimethoxyquinoxaline (344 mg, 1.5 mmole). After being heated at 80° C. overnight, the reaction mixture is concentrated. The residue is chromatographed on silica gel (50% ethyl acetate/hexane) to give 164 mg (23%) of a yellow solid (m.p. 158-159° C.). the reaction mixture is concentrated The residue is chromatographed on silica gel (50% ethyl acetate/hexane)
ソース ID: ord-c8fda7726bb64c24808edb3ca7167c2bPubChem References
化合物の公開データベース記録に掲載された情報源です。
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