HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 178429220, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | 2H-Indol-2-one, 5,6-diamino-1,3-dihydro-3,3-dimethyl- | HCID 13589237 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178429220 | HCID 178429220 | — |
Reaction Steps
3.00 g. (0.016 mole) 5,6-diamino-3,3-dimethylindolin-2-one are suspended in 100 ml. ethanol and mixed at ambient temperature with 1.82 g. (0.017 mole) cyanogen bromide and stirred for 2 hours. The solvent is removed in a vacuum and the residue is dissolved in ethanol, treated with active charcoal and the product precipitated out by the addition of acetone. The product is crystallised from acetone and a little ethanol to give 1.05 g. (22% of theory) of the title compound in the form of the hydrobromide; m.p. 300°-305° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04730003 |
| Source dataset | uspto-grants-1988_03 |
| ORD ID | ord-083791cb6af04aafa82eac936ee269af |
| Source note | uspto-grants-1988_03 |