HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 178523263, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Tributyltin azide | HCID 4984872 | — |
| Reactant | HCID 178511132 | HCID 178511132 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178523263 | HCID 178523263 | — |
Reaction Steps
A stirred solution of 2-(1H-indazol-3-yl)-1H-benzoimidazole-5-carboxylic acid (2-cyano-ethyl)-amide [150 mg, Example 246(s)] and azidotributyltin (2 ml) was heated at 95° C. for 24 hours. The reaction was cooled to ambient temperature and stirred for 2 hours with acetonitrile (20 ml), tetrahydrofuran (10 ml) and acetic acid (20 ml). The reaction mixture was washed with iso-hexane (6×80 ml) and concentrated in vacuo. The residue was subjected to preparative HPLC to give 2-(1H-indazol-3-yl)-1H-benzoimidazole-5-carboxylic acid [2-(2H-tetrazol-5-yl)-ethyl]-amide (35.9 mg) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08288425B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-3aa2cf098b644aba940d6c334c387c6f |
| Source note | uspto-grants-2012_10 |