참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chlorobenzoic Acid | HCID 6318 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Diethyl chlorophosphate | HCID 13139 | — |
| 반응물 | 2-Amino-3-(2-quinolon-3-yl)propionic acid | HCID 13342097 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(4-Chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid | HCID 13342103 | — |
반응 단계
1.2 Grams of 2-amino-3-(2-quinolon-3-yl)propionic acid and 0.8 ml of triethylamine were suspended in 10 ml of tetrahydrofuran, then under stirring condition at a room temperature, a solution containing 1.0 g of diethyl chlorophosphate in 10 ml of tetrahydrofuran was added dropwise thereto, and the reaction mixture was stirred at a room temperature for 3 hours. To this reaction mixture was added a solution containing 1.0 g of p-chlorobenzoic acid in 10 ml of tetrahydrofuran dropwise and the whole reaction mixture was further stirred at a room temperature for 10 hours. After completion of the reaction, the crystals precipitated were removed by filtration, the filtrate was concentrated and to the residue was poured a saturated sodium hydrogencarbonate aqueous solution, then extracted with chloroform. The organic layer was washed with water and a saturated sodium chloride aqueous solution and dried with sodium sulfare. The solvent was removed by distillation and the residue was recrystallized from ethanol-water to obtain 0.9 g of 2-(4-chlorobenzoylamino)-3-(2-quinolon-3-yl)propionic acid in the form of white powder product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | USRE034722 |
|---|
| 출처 데이터셋 | uspto-grants-1994_09 |
|---|
| ORD ID | ord-99ec18de92e04031a18330f50956821a |
|---|
| 출처 메모 | uspto-grants-1994_09 |
|---|