HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574261Generated: October 29, 2026
Tributyltin azide → HCID 178454218, compound
https://huagongshe.com/reaction/574261
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin azide | HCID 4984872 | — |
| Reactant | HCID 67144622 | HCID 67144622 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178454218 | HCID 178454218 | 54.4% |
Reaction Steps
{(R)-2-[5-[4-(3-cyano-benzyl)-piperazin-1-yl]-3-(2-fluoro-6-trifluoromethyl-benzyl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester (35 mg, 0.049 mmol), and azidotributyl tin (IV) (16 μl, 0.059 mmol) were dissolved at 120° C. for 10 hrs in toluene (1 mL) with stirring. The solution was cooled to room temperature, followed by the addition of azidotributyl tin (IV) (20 μl, 0.074 mmol) thereto and stirring at 120° C. for an additional 2 hrs. The solution was cooled to room temperature, diluted in dichloromethane, and washed with an aqueous saturated ammonium chloride solution and an aqueous saturated sodium chloride solution in the order. The organic layer thus formed was separated and concentrated, and the residue was purified using silica gel chromatography (eluent: dichloromethane/methanol, 6/1) and dried in a vacuum to afford 20 mg of the compound as a colorless oil (yield 54%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034850B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-96daa9c3cfb54d3fa32a55d4ea3e6d01 |
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| Source note | uspto-grants-2015_05 |
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