HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 178470708, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl (4-chloro-6-methylpyrimidin-5-yl)acetate | HCID 10954591 | — |
| Reactant | HCID 178445676 | HCID 178445676 | — |
| Solvent | Toluene water | HCID 22272177 | — |
| Product | HCID 178470708 | HCID 178470708 | — |
Reaction Steps
15.2 g (71 mmol) of methyl (4-chloro-6-methylpyrimidin-5-yl)acetate, 11.0 g (71 mmol) of cis-4-tert-butylcyclohexylamine and 20.2 g (0.2 mol) of triethylamine were heated at 80° to 90° C. for 6 hours without solvent. After cooling, the mixture was taken up in water/toluene and the organic phase was dried and concentrated. In the chromatography on silica gel (petroleum ether/ethyl acetate 1:1, then ethyl acetate/methanol 9:1), 5.3 g of chloropyrimidine starting material were first of all retained and then 10.0 g (27.7% of theory) of product were obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05852023 |
| Source dataset | uspto-grants-1998_12 |
| ORD ID | ord-59f59c62c84f402caf8a9d7bef42ea7b |
| Source note | uspto-grants-1998_12 |