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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 491844Generated: October 30, 2026

Sodium Bicarbonate → 5-tert-butyl-N-{3-[4-(5-ethyl-1-phenyl-1H-pyrazol-4-yl)-imidazol-1-yl]-4-methyl-phenyl}-3-methanesulfonylamino-2-methoxy-benzamide

https://huagongshe.com/reaction/491844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant5-Tert-butyl-3-methanesulfonylamino-2-methoxy-benzoic acid methyl esterHCID 57678863—
Reactant3-[4-(5-ethyl-1-phenyl-1H-pyrazol-4-yl)-imidazol-1-yl]-4-methyl-phenylamineHCID 57678880—
SolventTetrahydrofuranHCID 8028—
Product5-tert-butyl-N-{3-[4-(5-ethyl-1-phenyl-1H-pyrazol-4-yl)-imidazol-1-yl]-4-methyl-phenyl}-3-methanesulfonylamino-2-methoxy-benzamideHCID 1170012440.2%

Reaction Steps

3-[4-(5-Ethyl-1-phenyl-1H-pyrazol-4-yl)-imidazol-1-yl]-4-methyl-phenylamine (Example 3) (80 mg, 0.23 mmol) was dissolved in THF (5 mL) under N2 and 0.9 mL of 1 M LiHMDS (0.9 mmol) was slowly added. After stirring for 5 min, a solution of 73.5 mg (0.23 mmol) of 5-tert-butyl-3-methanesulfonylamino-2-methoxy-benzoic acid methyl ester (Example 1) in 5 mL of THF was added. The mixture was stirred at room temperature for 45 min, then saturated NaHCO3 (10 mL) was slowly added. The resulting mixture was then extracted with CH2Cl2 (100 mL). Chromatography (30 to 100% EtOAc in hexanes) provided the title compound as a tan foam (58 mg, 40%). ESI MS m/z 627 [C34H38N6O4S+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531560B2
Source datasetuspto-grants-2009_05
ORD IDord-9dfeb1ef5800428494cb680e8a31a91a
Source noteuspto-grants-2009_05