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HRID 271053作成日:2026年10月26日

Carbon Dioxide → 2-bromo-3-cyclohexyl-N-(dimethylsulfamoyl)-1H-indole-6-carboxamide

https://huagongshe.com/reaction/271053

反応式

関与物質

役割名称HCID仕込み量
反応物Carbon DioxideHCID 280—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物N,N-DimethylsulfamideHCID 134472—
反応物2-bromo-3-cyclohexyl-1H-indole-6-carboxylic acidHCID 514261—
溶媒TetrahydrofuranHCID 8028—
生成物2-bromo-3-cyclohexyl-N-(dimethylsulfamoyl)-1H-indole-6-carboxamideHCID 58765150—

反応条件

温度50 °C

反応手順

1,1′-Carbonyldiimidazole (1.17 g, 7.2 mmol) was added to a stirred solution of 2-bromo-3-cyclohexyl-1H-indole-6-carboxylic acid (2.03 g, 6.3 mmol) in THF (6 mL) at 22° C. The evolution of CO2 was instantaneous and when it slowed the solution was heated at 50° C. for 1 hr and then cooled to 22° C. N,N-Dimethylsulfamide (0.94 g, 7.56 mmol) was added followed by the dropwise addition of a solution of DBU (1.34 g, 8.8 mmol) in THF (4 mL). Stirring was continued for 24 hr. The mixture was partitioned between ethyl acetate and dilute HCl. The ethyl acetate layer washed with water followed by brine and dried over Na2SO4. The extract was concentrated to dryness to leave the title product as a pale yellow friable foam, (2.0 g, 74%, >90% purity, estimated from NMR). 1H NMR (300 MHz, DMSO-D6) δ ppm 1.28-1.49 (m, 3H) 1.59-2.04 (m, 7H) 2.74-2.82 (m, 1H) 2.88 (s, 6H) 7.57 (dd, J=8.42, 1.46 Hz, 1H) 7.74 (d, J=8.78 Hz, 1H) 7.91 (s, 1H) 11.71 (s, 1H) 12.08 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07452876B2
出典データセットuspto-grants-2008_11
ORD IDord-7f13c3e684254f29b09a1c23fc7b5936
出典メモuspto-grants-2008_11