HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 22063001, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Benzhydrylamine | HCID 7036 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 10821153 | HCID 10821153 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22063001 | HCID 22063001 | — |
Reaction Steps
A solution of benzhydrylamine (366 mg, 2.0 mmol) and 2,4,6-triaminopyrido[2,3-d]pyrimidine (350 mg, 2.0 mmol) in a mixture of DMF (40 mL) and glacial AcOH (4 mL) is treated with BH3.Et3N (75 mg, 6.6 mmol), and the mixture is stirred at room temperature overnight, then diluted with H2O (20 mL) to decompose any unreacted reducing agent. The solvents are evaporated under reduced pressure, and the residue is purified on a silica gel column using 5-15% CHCl3 in MeOH as the eluent. Pooling and evaporation of appropriate fractions yields the title compound, N-(2,4-diaminopyrido[2,3-d]pyrimidin-6-yl)benzhydrylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07056911B1 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-cc4555a984094c1495eec4b1bbdf1468 |
| Source note | uspto-grants-2006_06 |