HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 178492008, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 178492007 | HCID 178492007 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178492008 | HCID 178492008 | 89% |
Reaction Steps
To a suspension of 0.01 g 2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-4,5,6,7-tetrahydro-1H-imidazo[4,5-c]pyridine hydrochloride in 0.8 ml tetrahydrofurane were added at 0–4° C. 0.02 ml N-ethyldiisopropylamine and 0.002 ml acetyl chloride in 0.25 ml tetrahydrofurane. The mixture was refluxed over night, silicagel was added and the solvent was distilled off. The residue was transferred to a column prefilled with silicagel and was chromatographed with ethylacetate/methanol 95:5 to yield 0.009 g (89%) 1-[2-(4-methoxy-7-morpholin-4-yl-benzothiazol-2-yl)-1,4,6,7-tetrahydro-imidazo[4,5-c]pyridin-5-yl]-ethanone as yellow solid; M.p.: 155–157° C.; MS (ISP): m/e=414 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07122545B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-da8d62101015498eb5c8b3f5ff52667a |
| Source note | uspto-grants-2006_10 |