Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1095002생성일: 2026년 10월 26일
Pyridine → 3-(3-{[Bis-(2-hydroxy-propyl)-amino]-methyl}-benzoylamino)-naphthalene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1095002
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Diisopropanolamine | HCID 8086 | — |
| 반응물 | 3-(Chloromethyl)benzoic acid | HCID 241752 | — |
| 반응물 | 3-(3-Chloromethylbenzoylamino)-naphthalene-2-carboxylic acid methyl ester | HCID 66638116 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 3-(3-{[Bis-(2-hydroxy-propyl)-amino]-methyl}-benzoylamino)-naphthalene-2-carboxylic acid methyl ester | HCID 66637804 | — |
반응 단계
Subsequently, 3-(3-chloromethyl-benzoylamino)-naphthalene-2-carboxylic acid methyl ester (870 mg) was dissolved in anhydrous methylene chloride (15 ml). Pyridine (400 μl) and diisopropanolamine (compound B′) (1.0 g) were added to the solution at room temperature, and the mixture was then stirred at that temperature for 48 hr. After the completion of the reaction, distilled water was added thereto at room temperature, and the mixture was subjected to separatory extraction with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated under the reduced pressure. The residue was purified by column chromatography eluted with a hexane-acetone system to give 3-(3-{[bis-(2-hydroxy-propyl)-amino]-methyl}-benzoylamino)-naphthalene-2-carboxylic acid methyl ester as a useful intermediate (640 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08134015B2 |
|---|
| 출처 데이터셋 | uspto-grants-2012_03 |
|---|
| ORD ID | ord-b33e69d7d05747159e1ac4dc093c2c2f |
|---|
| 출처 메모 | uspto-grants-2012_03 |
|---|