HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 5-Bromo-2-methyl-8-(4-methylpiperazin-1-yl)-[1,2,4]triazolo[1,5-a]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-Bromo-2-methyl-8-(piperazin-1-yl)-[1,2,4]triazolo[1,5-a]pyrazine | HCID 58447057 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-Bromo-2-methyl-8-(4-methylpiperazin-1-yl)-[1,2,4]triazolo[1,5-a]pyrazine | HCID 58446984 | 76% |
Reaction Steps
A 100 mL round bottom flask was charged with 5-bromo-2-methyl-8-(piperazin-1-yl)-[1,2,4]-triazolo[1,5-a]pyrazine (0.5 g, 1.7 mmol), CH2Cl2 (20 mL), MeOH (10 mL), 40% aqueous formaldehyde (2 mL) and NaBH3(CN) (0.5 g, 8.0 mmol). The resulting solution was stirred at room temperature for 0.5 h. Work-up: the reaction mixture was poured into saturated aqueous NaHCO3 and extracted with CH2Cl2 (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 1-10% MeOH in CH2Cl2, to afford 0.4 g (76%) of the product as a yellow solid. MS m/z: 311 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08569300B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-7e7f697cf5fe49378143303cecd53064 |
| Source note | uspto-grants-2013_10 |