HuagongsheHuagongshe Chemistry Print Report · For research reference only
ethyl 2-(1H-1,3-benzodiazol-2-yl)acetate → HCID 136348951, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | ethyl 2-(1H-1,3-benzodiazol-2-yl)acetate | HCID 308071 | — |
| Reactant | HCID 22664648 | HCID 22664648 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136348951 | HCID 136348951 | — |
Reaction Steps
t-BuLi (3.1 eq) was added to ethyl 2-benzimidazol-2-ylacetate (1.0 eq) and 6-amino-2-(4-ethylpiperazinyl)benzenecarbonitrile (1.0 eq) in THF at 0° C. The reaction was stirred overnight. The resulting mixture was quenched with NH4Cl (aq, saturated) and extracted with EtOAc. The combined organic layers were washed with H2O and brine, dried over Na2SO4, filtered, and concentrated in vacuo to yield a brown solid. The crude material was triturated with CH2Cl2 and MeOH to provide a tan solid. LC/MS m/z 389.1 (MH+), Rt 1.80 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06800760B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-fb69ec674af2448c9aefac7a7487c9df |
| Source note | uspto-grants-2004_10 |