HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893915Generated: November 2, 2026
Tributyltin azide → HCID 178462870, compound
https://huagongshe.com/reaction/1893915
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributyltin azide | HCID 4984872 | — |
| Reactant | HCID 57606980 | HCID 57606980 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 178462870 | HCID 178462870 | 45% |
Reaction Steps
Tributyltin azide (660 μL, 2.41 mmol) was added to a flask charged with 2-amino-8-ethyl-4-methyl-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidine-6-carbonitrile (0.184 g, 0.803 mmol) in anhydrous toluene (5.0 mL). The reaction was fitted with a reflux condenser and heated to 140° C. under a nitrogen atmosphere. After 20 h, the reaction was cooled to room temperature and the precipitate collected by vacuum filtration and washed with absolute ethanol to give 2-amino-8-ethyl-4-methyl-6-(1H-tetrazol-5-yl)pyrido[2,3-d]pyrimidin-7(8H)-one (98 mg, 45% yield) as a light brown solid: 1H NMR (400 MHz, 20% DCl in D2O): δ 6.97 (s, 1H), 2.42 (q, J=7.2 Hz, 2H), 0.953 (s, 3H), −0.73 (t, J=7.2 Hz, 3H); MS (EI) for C11H11N8O: 271.0 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513266B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-03d5fd25a242449ba9e266d97e87cdaf |
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| Source note | uspto-grants-2013_08 |
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