HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylhydrazine → 4,6-dichloro-1-methyl-1H-pyrazolo(3,4-d)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | 2,4,6-Trichloro-5-pyrimidinecarboxaldehyde | HCID 10932746 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4,6-dichloro-1-methyl-1H-pyrazolo(3,4-d)pyrimidine | HCID 222247 | — |
Reaction Steps
To a solution of 2,4,6-trichloro-pyrimidine-5-carbaldehyde (3.7 g, 17.5 mmol) in EtOH (50 mL) cooled to −78° C. was added methyl hydrazine (0.93 mL, 17.5 mmol) and TEA (8 mL). The mixture was stirred for 30 minutes at −78 C then 2 hr at 0 C. The solution was concentrated in vacuo without heating. To the reduced volume solution was added EtOAc and the solution washed with a sat NaHCO3 solution and concentrated in vacuo without heating. Filtration over a small silica gel plug (2:1 EtOAc:Hex) and concentration afforded the desired product as a yellow solid. It should be noted that the reaction with aromatic hydrazine compounds can be conducted at 0° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08129371B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-259b631434fb4556b10bed0845f93446 |
| Source note | uspto-grants-2012_03 |