HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50852Generated: October 28, 2026
P-Anisidine → 4-N-(4-methoxyphenyl)pyrido[4,3-d]pyrimidine-4,7-diamine
https://huagongshe.com/reaction/50852
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | 7-Amino-4-methylthiopyrido[4,3-d]pyrimidine | HCID 10442562 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-N-(4-methoxyphenyl)pyrido[4,3-d]pyrimidine-4,7-diamine | HCID 5328062 | 25% |
Reaction Steps
A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (129 mg, 0.62 mmol) and 4-methoxyaniline ((0.15 g, 1.2 mmol) was in ethanol (5 mL) was heated at 40° C. for 16 h, and then reflux for 3 h. The reaction mixture was cooled to 0° C. overnignt, and the solid was colected by vacuum filtration and recrystalized from isopropanol to give 7-amino-4-(4-methoxyanilino)pyrido[4,3-d]pyrimidine (42 mg, 25%) as a yellow solid. 1H NMR (DMSO) δ 10.00 (1H, brs), 9.31 (1H, s), 8.35 (1H, s), 7.62 (2H, d, J=9.2 Hz), 6.96 (2H, d, J=9.2 Hz), 6.70 (2H, slbrs), 6.41 (1H, s), 3.77 (3H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06713484B2 |
|---|
| Source dataset | uspto-grants-2004_03 |
|---|
| ORD ID | ord-0e23e24b350049ec97d01f3e8aad66fa |
|---|
| Source note | uspto-grants-2004_03 |
|---|