Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2089690생성일: 2026년 10월 26일
Acetic Acid → [1-amino(4-{[(R)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl](5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]-triazol-3-yl)methyl]amino}phenyl)methylene]carbamic acid 2-methylallyl ester
https://huagongshe.com/reaction/2089690
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Methyl-allyl phenyl carbonate | HCID 15179082 | — |
| 반응물 | 4-{[(R)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl](5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]-triazol-3-yl)methyl]amino}benzamidine hydrochloride | HCID 136334035 | — |
| 용매 | Dimethyl Sulfoxide | HCID 679 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | [1-amino(4-{[(R)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl](5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]-triazol-3-yl)methyl]amino}phenyl)methylene]carbamic acid 2-methylallyl ester | HCID 136334036 | — |
반응 단계
To a mixture of 4-{[(R)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl](5-oxo-1-pyrimidin-2-yl-4,5-dihydro-1H-[1,2,4]-triazol-3-yl)methyl]amino}benzamidine hydrochloride (5.0 g, 9.41 mmol), potassium carbonate (2.6 g, 18.8 mmol), and dimethyl sulfoxide (15 mL), carbonic acid 2-methylallyl ester phenyl ester [CAS No. 138621-73-5] (1.57 g, 8.19 mmol) was added, and the resulting mixture was stirred at room temperature for 4 days. Ethyl acetate (100 mL) and water (200 mL) were added to the reaction solution, and the aqueous layer was collected. Acetic acid (1.62 mL, 28.2 mmol) was added dropwise to the aqueous layer with stirring, and the precipitated solid was filtered and sequentially washed with water (20 mL) and diethyl ether (20 mL). The solid obtained was suspended in ethyl acetate, filtered, and then dried under air flow. The dried solid was suspended in ethyl acetate (50 mL), and the suspension was stirred for 1 day. The suspension was filtered, and the solid obtained was washed with ethyl acetate and dried under air flow to obtain the captioned compound (4.87 g) as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08436009B2 |
|---|
| 출처 데이터셋 | uspto-grants-2013_05 |
|---|
| ORD ID | ord-82751cfed9674176a7c83b1e82b227e2 |
|---|
| 출처 메모 | uspto-grants-2013_05 |
|---|