HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 178458511, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 178458505 | HCID 178458505 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178458511 | HCID 178458511 | 35% |
Reaction Steps
To a suspension of 2-(5-amino-2-n-propoxyphenyl)-5-(5-1H-tetrazolyl)pyrimidin-4(3H)-one (0.50 g., 1.6 mmoles) in acetonitrile (40 ml.) was added 37% formaldehyde in water (1.32 ml., 16.0 mmoles). Sodium cyanoborohydride (0.302 g., 4.8 mmoles) was then added followed by glacial acetic acid (1.67 ml. The suspension was stirred at room temperature for 15 minutes and then heated under reflux for 3 hours. The mixture was cooled in an icebath. The precipitate was recrystallized from acetonitrile to give the title compound (0.19 g., 35%), m.p. 258°-259°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04082751 |
| Source dataset | uspto-grants-1978_04 |
| ORD ID | ord-87fb7fd4709848a6a30a710f596fa53d |
| Source note | uspto-grants-1978_04 |