HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-(-)-1-Aminoindan → HCID 89825842, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-(-)-1-Aminoindan | HCID 2733933 | — |
| Reactant | alpha-Cyclohexylcyclohexanemethanamine | HCID 10774245 | — |
| Reactant | 5-Fluoro-2-(trifluoromethyl)pyrimidine | HCID 13754255 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 89825842 | HCID 89825842 | 101.5% |
Reaction Steps
0.20 g (1.20 mmol) of 5-fluoro-2-(trifluoromethyl)pyrimidine, 0.225 g (1.69 mmol) of (1R)-2,3-dihydro-1H-inden-1-amine and 0.50 g (2.41 mmol) of dicyclohexylmethylamine in 1.5 ml of 1-methyl-2-pyrrolidone are heated in a closed cuvette in the microwave at 180° C. for 120 minutes (Biotage Initiator, http://www.biotage.com/DynPage.aspx?id=22001). The crude mixture obtained in this manner is applied to silica gel and purified by column chromatography using the mobile phase heptane/ethyl acetate. Concentration gives 0.34 g of N-[(1R)-2,3-dihydro-1H-inden-1-yl]-2-(trifluoromethyl)pyrimidine-5-amine (melting point 123.7° C., yield 96% at a purity of 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09375002B2 |
| Source dataset | uspto-grants-2016_06 |
| ORD ID | ord-b6033d8162e7421e8f0043ba556f7773 |
| Source note | uspto-grants-2016_06 |