Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 845613생성일: 2026년 10월 25일
Phenethyl bromide → 1-(2-Phenylethyl)-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide
https://huagongshe.com/reaction/845613
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenethyl bromide | HCID 7666 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ether hydrobromide | HCID 86739792 | — |
| 반응물 | HCID 178480237 | HCID 178480237 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-(2-Phenylethyl)-3-(1-methyl-4-piperidinyl)-1H-indazole hydrobromide | HCID 14032511 | 36% |
반응 단계
To a stirred mixture of 0.86 g of sodium hydride (50% oil dispersion) in 50 ml of dimethylformamide was added, dropwise, 3.0 g of 3-(1-methyl-4-piperidinyl)-1H-indazole in 15 ml of hot dimethylformamide. The reaction mixture was stirred at ambient temperature for 1 hr and then a solution of 3.33 g of (2-bromoethyl)benzene in 10 ml of dimethylformamide was added dropwise. The reaction mixture was stirred for 21/2 days at ambient temperature, cooled to 0° , and water was added dropwise. The mixture was extracted with ethyl acetate, washed with water, dried over anhydrous magnesium sulfate and the solvent was removed in vacuo to yield an oil. The oil was dissolved in ether and a saturated hydrogen bromide/ether solution was added dropwise. The resultant solid was recrystallized two times from ethanol to yield 2.0 g (36%) of product, mp 163°-164° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US04758668 |
|---|
| 출처 데이터셋 | uspto-grants-1988_07 |
|---|
| ORD ID | ord-401631fb0d944a8c9ea03ef704fc20da |
|---|
| 출처 메모 | uspto-grants-1988_07 |
|---|