HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397126Generated: October 29, 2026
Azido(trimethyl)stannane → HCID 178458916, compound
https://huagongshe.com/reaction/397126
Participants
| Role | Name | HCID | Charge |
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| 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 |
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| Patent number | US06608210B2 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-9e62aa45459140bd81886ded3344c155 |
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| Source note | uspto-grants-2003_08 |
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