HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1852492Generated: November 2, 2026
Sodium Bicarbonate → HCID 178516631, compound
https://huagongshe.com/reaction/1852492
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Tributyltin azide | HCID 4984872 | — |
| Reactant | HCID 56603173 | HCID 56603173 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178516631 | HCID 178516631 | — |
Reaction Steps
To an anhydrous DMF (5 mL) solution of 5-(3-cyanophenyl)-8,9,10,11-tetrahydronaphtho[2,1-b][1,4]diazepine-2,4(3H,5H)-dione (302 mg, 0.91 mmol) was added tri-n-butyltin azide (499 μL, 1.82 mmol). The mixture was stirred at 110° C. for 24 hours. The reaction mixture was cooled on standing, poured into saturated aqueous sodium hydrogen carbonate solution, and washed with ethyl acetate. After neutralization of the aqueous layer by addition of 1M hydrochloric acid, the layer was extracted with ethyl acetate, washed with purified water, and dried over anhydrous sodium sulfate. The solvent was removed by evaporation under reduced pressure. The residue was purified by chromatography (chloroform/methanol=95/5) to give the titled compound as slightly yellow powder (242 mg, yield 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08962613B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-f6641430b67e4468bae43277c4469083 |
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| Source note | uspto-grants-2015_02 |
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