HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 494352Generated: October 29, 2026
Azido(trimethyl)stannane → HCID 178458916, compound
https://huagongshe.com/reaction/494352
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | HCID 15654675 | HCID 15654675 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178458916 | HCID 178458916 | — |
Reaction Steps
A mixture of ethyl 1-[(2′-cyanobiphenyl-4-yl)methyl]-2-propoxybenzimidazole-7-carboxylate (0.69 g) and trimethyltin azide (0.7 g) in toluene (15 ml) was heated for 4 days under reflux. The reaction mixture was concentrated to dryness and to the mixture was added methanol (20 ml) and 1N-HCl (10 ml). After stirring at room temperature for 30 minutes, the mixture was adjusted to pH 3-4 with 1N NaOH. After removal of the solvent, the residue was extracted with chloroform-water. The organic layer was washed with water and dried, and the solvent was evaporated to dryness to give a syrup. The syrup was purified by column chromatography on silica gel to give crystals. Recrystallization from ethyl acetate-benzene afforded colorless crystals (0.31 g, 43%), m.p. 157-159° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07538133B2 |
|---|
| Source dataset | uspto-grants-2009_05 |
|---|
| ORD ID | ord-7305bd1d0cac44ecab6f715082de1907 |
|---|
| Source note | uspto-grants-2009_05 |
|---|