HuagongsheHuagongshe Chemistry Print Report · For research reference only
Guanidine Hydrochloride → 4'-Methyl-2-methylsulfanyl-[4,5']bipyrimidinyl-2'-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Guanidine Hydrochloride | HCID 5742 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Dimethylamino-3-(2-methylsulfanyl-pyrimidin-4-yl)-but-3-en-2-one | HCID 67983534 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4'-Methyl-2-methylsulfanyl-[4,5']bipyrimidinyl-2'-ylamine | HCID 67983866 | 80% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
To a solution of 4-Dimethylamino-3-(2-methylsulfanyl-pyrimidin-4-yl)-but-3-en-2-one (18) (1.02 g, 4.30 mmol) in DMF (14 mL) was added K2CO3 (1.782 g, 12.89 mmol) and Guanidine HCl (0.616 g, 6.45 mmol) and the resulting suspension was stirred at 120° C. for 1 hour. The DMF was evaporated and the crude residue partitioned between water and ethyl acetate. The organic layer was washed with water and brine, dried with sodium sulfate, and concentrated. The crude residue was purified by flash chromatography with a gradient of 1-12% MeOH in DCM to give the desired product as a light yellow solid (800 mg, 80%). MS (ES+): m/z=234.3/235.4 (100/20) [MH+]. HPLC: tR=1.01 minutes over 3 minutes. Purity: 70% [HPLC (LC/MS) at 220 nm].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08685993B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-4a4025b024184db8a66bd314a14fe5eb |
| Source note | uspto-grants-2014_04 |