Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Bromomethyl 4-methoxyphenyl ketone → 5-Amino-2-(1-[4-methoxyphenylcarbonylmethyl]benzimidazol-2-yl)-pyrazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 5-amino-2-(1H-benzimidazol-2-yl)pyrazole | HCID 57464472 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 5-Amino-2-(1-[4-methoxyphenylcarbonylmethyl]benzimidazol-2-yl)-pyrazole | HCID 57494334 | — |
반응 단계
A suspension of 5-amino-2-(1H-benzimidazol-2-yl)pyrazole (0.10 g, 0.5 mmol), p-methoxyphenacyl bromide (0.204 g, 0.9 mmol) and dry potassium carbonate (0.173 g, 1.25 mmol) is stirred at room temperature for 16 hours. The mixture is diluted with water and the product extracted with ethyl acetate. The product is purified by chromatography on silicagel. M.p. 136-140° C., 1H-NMR (400 MHz, d6-DMSO): 8.04 (d, 2H); 7.58 (m, 2H); 7.28 (m, 3H); 7.11 (d, 2H); 6.84 (s, 2H); 6.26 (s, 2H); 5.39 (d, 1H); 3.87 (s, 3H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07423157B2 |
| 출처 데이터셋 | uspto-grants-2008_09 |
| ORD ID | ord-f8b0f03890c64aedba67ef2fd6510344 |
| 출처 메모 | uspto-grants-2008_09 |