HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminobenzonitrile → HCID 178507210, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminobenzonitrile | HCID 72913 | — |
| Reactant | HCID 22664674 | HCID 22664674 | — |
| Product | HCID 178507210 | HCID 178507210 | — |
Reaction Steps
The title compound was synthesized as described in Example 46, using ethyl 2-(5-morpholin-4-ylimidazolo[5,4-b]pyridin-2-yl)acetate and 2-aminobenzenecarbonitrile, with a modified workup procedure. After quenching with a saturated aqueous ammonium chloride solution, the two phases were separated and the aqueous phase extracted with EtOAc. Upon standing, a solid formed and precipitated out of the organic extracts. The precipitate, a dark brown solid, was filtered off and dried. Purification by reverse phase chromatography afforded the desired product as a reddish solid. LC/MS m/z 363.2 (MH+), Rt 2.20 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07825132B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-8757c55deab1482b96f8d9469fd3cc3a |
| Source note | uspto-grants-2010_11 |