Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 239960생성일: 2026년 10월 26일
Triethylamine → Methyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate
https://huagongshe.com/reaction/239960
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Propylphosphonic anhydride | HCID 111923 | — |
| 반응물 | Benzoic acid, 4-amino-3,5-dimethyl-, methyl ester | HCID 11030398 | — |
| 반응물 | 6-Chloro-3-methylpyridine-2-carboxylic acid | HCID 46941470 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Methyl 4-[(6-chloro-3-methyl-pyridine-2-carbonyl)amino]-3,5-dimethyl-benzoate | HCID 86707309 | 81% |
반응 단계
To a solution of 6-chloro-3-methyl-pyridine-2-carboxylic acid (0.70 g, 4.093 mmol, see preparation 1) in CH2Cl2 (6 mL) at 0° C. are added methyl 4-amino-3,5-dimethylbenzoate (0.74 g, 4.093 mmol, see preparation 12), and triethylamine (0.83 g, 8.187 mmol). After stirring the reaction mixture for 10 minutes, 1-propanephosphonic acid cyclic anhydride (50% solution in ethyl acetate, 2.60 g, 8.187 mmol) is added via syringe and stirred at ambient temperature. After 12 hours, the solvent is removed under reduced pressure and the residue is diluted with water and extracted with ethyl acetate. The organic layers are combined and dried over anhydrous Na2SO4, filtered, and concentrated under reduced pressure. The resulting residue is purified by flash chromatography (silica gel) using a gradient of 0-40% ethyl acetate in hexanes to give the title compound as an off-white solid (1.10 g, 81%). Mass spectrum (m/z): 333.2 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08642768B2 |
|---|
| 출처 데이터셋 | uspto-grants-2014_02 |
|---|
| ORD ID | ord-55bc217fa3934dc9b7500163da0ad06d |
|---|
| 출처 메모 | uspto-grants-2014_02 |
|---|