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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796335Generated: November 1, 2026

HCID 11338407, compound → HCID 11476994, compound

https://huagongshe.com/reaction/1796335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11338407HCID 11338407—
ReactantHCID 178418255HCID 178418255—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11476994HCID 11476994—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030145B2
Source datasetuspto-grants-2006_04
ORD IDord-d94a12a0fff64229b3692ad239cf58d4
Source noteuspto-grants-2006_04