HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 178453907, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 2-tert-Butyl-4-cyclobutyl-6-(piperazin-1-yl)pyrimidine | HCID 66673390 | — |
| Reactant | HCID 178453924 | HCID 178453924 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178453907 | HCID 178453907 | 86% |
Reaction Steps
A mixture of 2-tert-butyl-4-cyclobutyl-6-(piperazin-1-yl)pyrimidine (7.16 g, 26.1 mmol) and tert-butyl trans-4-(2-oxoethyl)cyclohexylcarbamate (6 g, 24.86 mmol) in DCE (100 ml) was stirred at room temperature for 10 min. AcOH and sodium triacetoxyhydroborate (7.90 g, 37.3 mmol) were added. After 4 h, water was added. The aqueous layer was extracted with methylene chloride (3×50 mL). The combined organic layers were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to give the title compound as a yellow oil of (11.2 g, 21.29 mmol, 86% yield) which was used next step without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09388141B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-25b6ffdfaac543a9813b78e308bd8429 |
| Source note | uspto-grants-2016_07 |