참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 5-Bromo-1-methyl-1H-imidazole | HCID 1515258 | — |
| 반응물 | N-Methoxy-N-methyl-1,3-thiazole-5-carboxamide | HCID 25307138 | — |
| 반응물 | HCID 178418443 | HCID 178418443 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (1-Methyl-1H-imidazol-5-yl)(thiazol-5-yl)methanone | HCID 86715592 | — |
반응 단계
To a solution of 5-bromo-1-methyl-1H-imidazole (1.14 g, 7.11 mmol) in DCM was added ethyl magnesium bromide (2.34 mL, 7.11 mmol; 3.0 M in diethyl ether) dropwise over a 10 minute period. The resulting pale yellow solution was stirred at room temperature for 15 minutes, cooled in an ice bath to 0° C. and N-methoxy-N-methylthiazole-5-carboxamide (1.02 g, 5.92 mmol, Intermediate 11: step a) dissolved in DCM (3 mL) was added dropwise. The cold bath was removed and the reaction mixture stirred at room temperature for 48 hours. To the resulting yellow suspension was added water followed by 6 M aqueous HCl to a neutral pH (pH=6-7). The aqueous mixture was extracted with DCM, dried over Na2SO4, filtered and concentrated. Et2O was added and the mixture sonicated. The precipitate was collected by filtration and dried to provide the title compound as a tan solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US09290476B2 |
|---|
| 출처 데이터셋 | uspto-grants-2016_03 |
|---|
| ORD ID | ord-605fe22491404975a4da403d95aa5b3f |
|---|
| 출처 메모 | uspto-grants-2016_03 |
|---|