HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631867Generated: October 30, 2026
Hydrochloric Acid → HCID 178527472, compound
https://huagongshe.com/reaction/631867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Dibutyltin oxide | HCID 61221 | — |
| Reactant | Azidotrimethylsilane | HCID 78378 | — |
| Reactant | N-(2-Cyano-3-cyclopropylphenyl)-benzenesulfonamide | HCID 68296410 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 178527472 | HCID 178527472 | 65.5% |
Reaction Steps
N-(2-Cyano-3-cyclopropylphenyl)-benzenesulfonamide (Intermediate 9, 0.052 g), azidotrimethyl-silane (0.087 g) and dibutyltin oxide (0.038 g) were suspended in 1,2-dichloroethane (3 mL). The mixture was heated by microwave irradiation at 140° C. for 45 minutes. Six further aliquots of azidotrimethylsilane (0.174 g) were added and after each addition the mixture was heated by microwave irradiation at 140° C. for 60 minutes. The reaction mixture was acidified to pH 1 using 1N hydrochloric acid, and then extracted with ethyl acetate. The combined organic extracts were dried with magnesium sulfate, filtered and the filtrate was evaporated under vacuum. The residue was triturated with a mixture of pentane and cyclohexane and the solid was collected by filtration, to give the title compound as a white solid (0.039 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321740B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-8799f27009a34ac4ba55facae8bd241e |
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| Source note | uspto-grants-2016_04 |
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