HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796335Generated: November 1, 2026
HCID 11338407, compound → HCID 11476994, compound
https://huagongshe.com/reaction/1796335
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 11338407 | HCID 11338407 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11476994 | HCID 11476994 | — |
Reaction Steps
4-[6-Methyl-2-(2,4,6-trimethylphenylamino)-pyridine-3-sulfonyl]-benzaldehyde, prepared as described in Example 52, (100 mg, 0.25 mmol) was dissolved in dry THF and cooled to 0° C. To the solution was added a 1 M solution of PhMgBr in THF (0.63 mL, 0.63 mmol) and the reaction was stirred at 25° C. for 2 h, quenched with water and neutralized with 10% HCl and extracted with EtOAc (100 mL). The EtOAc was washed with brine, dried and stripped in vacuo. The residue was purified by silica gel chromatography (20% EtOAc/hexanes eluent) to give 15 mg {4-[6-methyl-2-(2,4,6-trimethylphenylamino)-pyridine-3-sulfonyl]-phenyl}-phenyl-methanol as an amorphous solid. mass spec. (AP+): m/z 473 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030145B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-d94a12a0fff64229b3692ad239cf58d4 |
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| Source note | uspto-grants-2006_04 |
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