HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → Anagrelide Hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | Ethyl 2-((6-amino-2,3-dichlorobenzyl)amino)acetate | HCID 9814186 | — |
| Solvent | 2-Methoxyethanol | HCID 8019 | — |
| Product | Anagrelide Hydrochloride | HCID 135413494 | 31% |
Reaction Steps
A solution of cyanogen bromide (3.2 g, 0.030 mol) in 100 ml. 2-methoxyethanol was added to a solution of N-(6-amino-2,3-dichlorobenzyl)glycine ethyl ester (8.2 g, 0.030 mol) in 250 ml. 2-methoxyethanol. The solution was stirred at room temperature for 1 hour, heated at reflux for 22 hours, and cooled. The precipitate was filtered off, washed with ether and air dried to give 3.11 gms. of the crude title product (31% yield as the hydrobromide salt). Recrystallization from ethanolic HCl gave the pure title product in 71% recovery (22% overall yield); m.p. >250°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04146718 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-56be5e26d86e45a2bf84af2e8d3aedad |
| Source note | uspto-grants-1979_03 |