HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → Quinazolin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Hydrate;hydrochloride | HCID 21885828 | — |
| Reactant | ethyl-N-(6-amino-2,3-dichlorobenzyl)glycine | HCID 67080112 | — |
| Reactant | Anagrelide | HCID 135409400 | — |
| Product | Quinazolin-2-amine | HCID 178508286 | — |
Reaction Steps
Commercially, as discussed in U.S. Pat. No. 5,801,245 and as shown in FIG. 1, Anagrelide has been prepared as the hydrochloride monohydrate (compound IV) from the intermediate, ethyl N-(6-amino-2,3-dichlorobenzyl)glycine (compound I) by reaction with cyanogen bromide in hot alcohol solution, or, preferentially, by reaction with cyanogen bromide in an aprotic solvent to give the iminoquinazoline intermediate (compound II) which is isolated and then reacted with a base in a hot solution of alcohol to form Anagrelide base (compound III).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06653500B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-cfab49f40e6e4e44a0f2973c0270664c |
| Source note | uspto-grants-2003_11 |