참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dimethylformamide | HCID 6228 | — |
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | Oxalyl chloride | HCID 65578 | — |
| 반응물 | 4-Fluoro-1H-indole-7-carbonitrile | HCID 22473022 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-fluoro-3-formyl-1H-indole-7-carbonitrile | HCID 59146179 | 85.1% |
반응 단계
To a solution of (COCl)2 (16.0 g) in DCM (200 mL) at 0° C. was added a solution of DMF (6 mL) in DCM (50 mL) dropwise. Half an hour later, a solution of 4-fluoro-1H-indole-7-carbonitrile (D41) (11.0 g) in DCM (60 mL) was added. The reaction was allowed to warm to RT to form a yellow precipitate. After 6 h the solvent was removed by evaporation. Then THF (100 mL) and 2M aqueous NaOH (100 L) were added to the residue obtained above. After being stirred for about 1 hour, EtOAc (1 L) was added. The organic phase was separated and the aqueous phase was extracted with EtOAc. The combined organic solution was dried over anhydrous sodium sulfate. The dried solution was concentrated to afford 4-fluoro-3-formyl-1H-indole-7-carbonitrile (D42) as a yellow solid (11.0 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08217028B2 |
|---|
| 출처 데이터셋 | uspto-grants-2012_07 |
|---|
| ORD ID | ord-df697b7135ed4f2ea17eb24c2e6d36aa |
|---|
| 출처 메모 | uspto-grants-2012_07 |
|---|