HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetonitrile → HCID 16059409, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetonitrile | HCID 7856 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 16059348 | HCID 16059348 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 16059409 | HCID 16059409 | 14% |
Reaction Steps
To a stirred solution of 40 mg (0.101 mmol) of 1-[1-(6-Chloro-1H-indole-3-carbonyl)-piperidin-4-yl]-1,3-dihydro-benzoimidazol-2-one (the preparation of which has been described in example 18) in 5 ml DMF was added 4.2 mg (0.105 mmol) NaH (60% in oil). The mixture was stirred at RT for 30 min. and then 8.3 mg (0.11 mmol) of chloro-acetonitrile was added. The mixture was stirred an additional hour and then poured onto water and extracted with ethyl acetate. The combined organic phases were dried over Na2SO4 and concentrated in vacuo. Preparative HPLC afforded 6 mg (14%) of {6-Chloro-3-[4-(2-oxo-2,3-dihydro-benzoimidazol-1-yl)-piperidine-1-carbonyl]-indol-1-yl}-acetonitrile as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07803815B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-3fe02dac9e4b4e96b6d83f1764b5e407 |
| Source note | uspto-grants-2010_09 |