HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Heptanamine → HCID 58298342, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Heptanamine | HCID 38665 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 58298337 | HCID 58298337 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 58298342 | HCID 58298342 | 74.4% |
Reaction Steps
A mixture of 8-(4-bromo-2,6-dimethyl-phenyl)-4-chloro-2-methyl-pyrrolo[1,2-a]pyrimidine-6-carbonitrile (30.0 g), 1-propyl-butylamine (18.5 g), N,N-diisopropylethylamine (15.5 g) in ethanol (90 mL) was heated at reflux for 2 h. The reaction mixture was cooled to room temperature, poured into a saturated aqueous sodium hydrogencarbonate, and then extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to give a solid. The solid was washed with diisopropylether to give 8-(4-bromo-2,6-dimethyl-phenyl)-2-methyl-4-(1-propyl-butylamino)-pyrrolo[1,2-a]pyrimidine-6-carbonitrile (27.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106194B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-0a46d291187c47728b048b5d74e4c735 |
| Source note | uspto-grants-2012_01 |