HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248414Generated: November 1, 2026
Azido(trimethyl)stannane → HCID 178439912, compound
https://huagongshe.com/reaction/248414
Participants
| Role | Name | HCID | Charge |
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| Reactant | Azido(trimethyl)stannane | HCID 5104973 | — |
| Reactant | HCID 19759325 | HCID 19759325 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | HCID 178439912 | HCID 178439912 | 86.7% |
Reaction Steps
A mixture of 3-[4-(2-cyano-3-furyl)benzyl]-7-methyl-2-propyl-3H-imidazo[4,5-b]pyridine (540 mg) and trimethyltin azide (1.095 g) in xylene (10 ml) was stirred at 125° C. for 24 hours. The mixture was concentrated in vacuo. The residue was dissolved in methanol (15 ml) and the methanolic solution was treated with 8.9N methanolic hydrogen chloride (1 ml) for one hour at ambient temperature. The mixture was adjusted to pH 5 with aqueous 1N sodium hydroxide solution and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel (elution by dichloromethane/methanol=15/1-8/1) to yield 7-methyl-2-propyl-3-[4-[2-(1H-tetrazol-5-yl)-3-furyl]benzyl]-3H-imidazo[4,5-b]pyridine (525 mg) as an amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05210092 |
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| Source dataset | uspto-grants-1993_05 |
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| ORD ID | ord-dc837fe992194e2886e9fee1ee5a91b2 |
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| Source note | uspto-grants-1993_05 |
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