HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanogen Bromide → HCID 57678340, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanogen Bromide | HCID 10476 | — |
| Reactant | HCID 67023482 | HCID 67023482 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 57678340 | HCID 57678340 | — |
Reaction Steps
A solution of 4-[(5-amino-2-phenoxy-pyridin-4-ylmethyl)-amino]-N-(1-(R)-tert-butoxymethyl-2-morpholin-4-yl-2-oxo-ethyl)-4-(S)-cyclohexyl-butyramide (0.37 g, 0.6 mmol) and BrCN (3M in CH2Cl2, 0.25 mL) in EtOH (20 mL) was stirred at room temperature overnight. The EtOH was evaporated to yield an oil, which was purified by Gilson HPLC to yield 4-(2-amino-6-phenoxy-4H-pyrido[3,4-d]pyrimidin-3-yl)-N-(1-(R)-tert-butoxymethyl-2-morpholin-4-yl-2-oxo-ethyl)-4-(S)-cyclohexyl-butyramide as a white solid, as its corresponding TFA salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531545B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-0a52000b14ab4f038d765028c00f7259 |
| Source note | uspto-grants-2009_05 |