Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Hydrochloric Acid → HCID 178522657, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Hydrochloric Acid | HCID 313 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| 반응물 | Calcium Chloride | HCID 5284359 | — |
| 반응물 | 3-Bromo-4-methoxy-2-(1-methylethoxy)benzoic acid | HCID 14276515 | — |
| 반응물 | HCID 178509299 | HCID 178509299 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | HCID 178522657 | HCID 178522657 | — |
반응 단계
A mixture of 1.28 g (4.43 mmol) 3-bromo-4-methoxy-2-(1-methylethoxy)benzoic acid (prepared in Step 3) and 0.83 g 5.12 g (5.12 mmol) of 1,1'-carbonyldiimidazole in 15 ml of acetonitrile is warmed at reflux under nitrogen atmosphere (or CaCl2 filled drying tube) for one hour. The reaction mixture is treated with 1.07 g (10.62 mmol) of triethylamine and 0.44 g (5.17 mmol) of anhydrous 5-aminotetrazole. The resulting mixture is warmed at reflux for 30 hours. The reaction mixture is then poured onto 180 g of ice water and acidified with aqueous 10% HCl and filtered to give 1.32 g (1.58 theor., 84%) of 3-bromo-4-methoxy-2- 1-methylethoxy)-N-1H-tetrazol-5-ylbenzamide as a white solid having melting point 255°-256° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04764525 |
| 출처 데이터셋 | uspto-grants-1988_08 |
| ORD ID | ord-407b8cae0d874901b9c8ba61bc41af52 |
| 출처 메모 | uspto-grants-1988_08 |