HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1581560Generated: November 2, 2026
Propargyl alcohol → HCID 178522931, compound
https://huagongshe.com/reaction/1581560
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178522930 | HCID 178522930 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178522931 | HCID 178522931 | — |
Reaction Steps
A mixture of 2-bromo-N-(4-chlorobenzyl)-8-hydroxypyrido[3,2-d]pyrimidine-7-carboxamide (Preparation 6, 1.97 g), (Ph3P)2PdCl2 (175 mg), and triethylamine (5.0 mL) in DMF (50 mL) is heated to 90° C. Propargyl alcohol (2.5 mL) is slowly added to the mixture over 20 h. The reaction mixture is allowed to cool to room temperature, poured into saturated aqueous NH4Cl solution (200 mL), and extracted with ethyl acetate (3×100 mL). The combined organic layers are dried (MgSO4) and concentrated. The crude product is purified by column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06730682B2 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-210fc15bc064469f880c4796cf18c38c |
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| Source note | uspto-grants-2004_05 |
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