Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Triethylamine → 2-(1-Benzothien-2-yl)-5-[(2-bromobutanoyl)amino]benzamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Bromobutanoyl bromide | HCID 117293 | — |
| 반응물 | 5-Amino-2-(1-benzothien-2-yl)benzamide | HCID 59428475 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-(1-Benzothien-2-yl)-5-[(2-bromobutanoyl)amino]benzamide | HCID 59428488 | — |
반응 단계
5-Amino-2-(1-benzothien-2-yl)benzamide (Example 8A, 886 mg) and triethylamine (650 mg) are introduced into DCM (20 ml) at 0° C., and 2-bromobutyryl bromide (1000 mg) is slowly added. The reaction mixture is warmed to RT and then stirred overnight. The reaction mixture is subsequently diluted with DCM (100 ml) and washed with 5% strength potassium bisulfate solution (twice 50 ml), dried (sodium sulfate) and concentrated in a rotary evaporator. The residue is chromatographed on silica gel (eluent cyclohexane-ethyl acetate 10:1 to 1:1). After concentration of the relevant fraction, 607 mg (47% of theory) of product are isolated.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07776922B2 |
| 출처 데이터셋 | uspto-grants-2010_08 |
| ORD ID | ord-5de46038a5c34b34aec8ba454fa68e3f |
| 출처 메모 | uspto-grants-2010_08 |