HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 20291421, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 20291381 | HCID 20291381 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20291421 | HCID 20291421 | — |
Reaction Steps
Sodium cyanoborohydride (1.2 gm., 0.019 mole) is added to a stirred solution of 8-bromo-6-(m-aminophenyl)imidazo-[1,5-d]-as-triazine-4(3H)-one, aqueous formaldehyde (5 ml., 37%) in acetonitrile (110 ml.). The reaction mixture is stirred for 15 minutes then acetic acid is added to adjust the pH of the reaction mixture to 7. The reaction mixture is stirred for 45 minutes while the pH of the mixture is maintained at 7 with acetic acid being added as needed. The solvent is then evaporated in vacuo, the residual oil is added to 2 N potassium hydroxide (150 ml.), and crystallizes. The product is washed with water, and recrystallized from acetone-water, m.p. 206° C.(d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04168964 |
| Source dataset | uspto-grants-1979_09 |
| ORD ID | ord-c9c067e360be4270a19a862ceb40f89c |
| Source note | uspto-grants-1979_09 |