Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | CID 6432229 | HCID 6432229 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | HCID 178509104 | HCID 178509104 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | CID 86697018 | HCID 86697018 | 46.6% |
Reaction Steps
Sodium nitrite (2.88 g, 42 mmol) was added portionwise to cHCl (314 mL) at −15° C. and stirred for 15 min. 3-phenyl-4-(2-phenylethynyl)-1H-pyrazol-5-amine (5.4 g, 21 mmol) was added as a solid, followed by the addition of CH2Cl2 (10 mL). The reaction mixture was allowed to warm up and stirred at room temperature for 1 h. The reaction mixture was diluted with CH2Cl2 (44 mL) and NaCl (2.7 g) was added. The reaction mixture was heated to 50° C. for 1 d. The layers were separated and the organic layer was washed with water, dried (phase separator cartridge) and concentrated in vacuo. The residue was purified by column chromatography (silica gel, iso-hexanes/ethyl acetate 4:1, then CH2Cl2/ethyl acetate 1:0 to 4:1) yielding the title compound as a solid (3.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227976B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-b815a9652b30464fb5a2d3e5dccadb75 |
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| Source note | uspto-grants-2016_01 |
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