HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diphenylamine → N-[(2,4-Diaminopyrido[2,3-d]pyrimidin-6-yl)methyl]-N,N-diphenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diphenylamine | HCID 11487 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Diamino-6-bromomethylpyrido[2,3-d]pyrimidine hydrobromide | HCID 22063009 | — |
| Product | N-[(2,4-Diaminopyrido[2,3-d]pyrimidin-6-yl)methyl]-N,N-diphenylamine | HCID 9798129 | — |
Reaction Steps
X=N; W=CH2; Z=non-linked hydrogens on each phenyl group; Z=CH2; m=n=0) is prepared similarly as disclosed in Example 1 above by using N,N-diphenylamine (1.3 g, 0.77 mmol), NaH (50 mg, 2.1 mmol), and 2,4-diamino-6-bromomethylpyrido[2,3-d]pyrimidine hydrobromide (100 mg, 0.3 mmol). The product can be purified by chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07056911B1 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-c1de875673e646bbb342a425ed15b3e4 |
| Source note | uspto-grants-2006_06 |