HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → 2-(2-nitro-1H-imidazol-1-yl)-N-(2-fluoro-allyl)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Isobutyl chloroformate | HCID 62365 | — |
| Reactant | 2-(2-Nitroimidazol-1-yl)acetic acid | HCID 327544 | — |
| Reactant | 2-Fluoroprop-2-en-1-amine hydrochloride | HCID 16723704 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-(2-nitro-1H-imidazol-1-yl)-N-(2-fluoro-allyl)acetamide | HCID 21111685 | 50% |
Reaction Steps
N-methylmorpholine (1.01 g, 10 mmol) was added to 2-(2-nitro-1H-imidazol-1-yl)-acetic acid (1.71 g, 10 mmol) in 150 mL of dry THF under nitrogen at 0° C. and stirred for 10 minutes. Isobutyl chloroformate (1.43 mL, 11 mmol) was added. After 30 minutes, 2-fluoro allyl amine hydrochloride (1.23 g, 11 mmol) and N-methylmorpholine (1.21 g, 12 mmol) was added to the solution and the mixture was stirred at room temperature overnight. The solution was filtered and the organic solvent evaporated to give a yellow solid. Purified by column afforded a light yellow solid (1.1 g, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432295B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-7ff87455f0c2433bb8541c6fef7d8231 |
| Source note | uspto-grants-2008_10 |