Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) → Ethyl (5-chloro-4-(5-fluoro-2-benzothiazolyl)amino-2-fluorophenyl)acetate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1) | HCID 466102 | — |
| 반응물 | Ethyl 4-amino-5-chloro-2-fluorophenylacetate | HCID 17858807 | — |
| 반응물 | 2-Bromo-5-fluorobenzo[d]thiazole | HCID 17859396 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | Ethyl (5-chloro-4-(5-fluoro-2-benzothiazolyl)amino-2-fluorophenyl)acetate | HCID 58778765 | 33% |
반응 단계
In xylene (5 ml), 2-bromo-5-fluorobenzothiazole (548 mg, 2.36 mmol), ethyl 4-amino-5-chloro-2-fluorophenylacetate (547 mg, 2.36 mmol), and pyridinium p-toluenesulfonate (PPTS) (178 mg, 0.71 mmol) were heated under reflux for 3 hours. After cooling, the reaction mixture was distilled under reduced pressure to remove the solvent. The residue was purified by chromatography on a silica gel column, whereby from n-hexane/ethyl acetate (7:1, v/v) eluate fractions, ethyl (5-chloro-4-(5-fluoro-2-benzothiazolyl)amino-2-fluorophenyl)acetate (298 mg, 33%) was obtained as a pale yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07157487B2 |
| 출처 데이터셋 | uspto-grants-2007_01 |
| ORD ID | ord-85eddbaed34b4d8eb09ca2a0baae7bdd |
| 출처 메모 | uspto-grants-2007_01 |