HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formic Acid → 7-Amino-2-benzylaminopyrido[4,3-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 2,4-Diamino,5-cyanopyridinium acetate | HCID 22736804 | — |
| Solvent | Water | HCID 962 | — |
| Product | 7-Amino-2-benzylaminopyrido[4,3-d]pyrimidine | HCID 22736810 | 73.3% |
Reaction Conditions
| Temperature | 200 °C |
|---|
Reaction Steps
A mixture of 2,4-diamino,5-cyanopyridinium acetate (8.78 g, 45 mmol), formic acid (10.66 g, 0.204 mol) and benzylamine (45 mL, 0.41 mol) is heated at 200° C. under N2 for 2 h. Upon cooling, it solidifies. Water (500 mL) is added and the gummy solid/water mixture is stirred for −20 min. at 0° C. The liquid is decanted. The solid is washed with water and then recrystallized from isopropanol (25 mL). After drying in a vacuum oven overnight, 7-amino-2-benzylaminopyrido[4,3-d]pyrimidine (8.29 g, 73%) is obtained as a light yellow solid. 1H NMR (DMSO) δ 9.10 (1H, s), 8.85 (1H, t, J=5.8 Hz), 8.25 (1H, s), 7.21-7.36 (5H, m), 6.46 (2H, brs), 6.35 (1H, s), 4.74 (2H, d, J=6.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455534B2 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-2906ff0bd38044f28dc09f3f53cd4a2a |
| Source note | uspto-grants-2002_09 |