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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480844Generated: November 1, 2026

Sodium Hydroxide → HCID 89996074, compound

https://huagongshe.com/reaction/1480844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium bis(trimethylsilyl)amideHCID 2724254—
ReactantHCID 89996145HCID 89996145—
ReactantHCID 89996185HCID 89996185—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89996074HCID 8999607448%

Reaction Steps

N-(2-Methoxy-4-(1-methyl-1H-pyrazol-4-yl)phenyl)formamide (Preparation 56, 50 mg 0.21 mmole) was stirred in THF (1 mL). Sodium hexamethyldisilazide (0.25 mL of 1M solution in THF) was added and the reaction stirred at room temperature for 20 minutes. 8-Chloro-6-cyclopropyl-2-(methylsulfonyl)pyrido[3,4-d]pyrimidine (Preparation 179, 80 mg, 0.28 mmole) was added as a suspension in THF (1.5 mL) and the reaction was stirred at room temperature for 80 minutes. Methanol (1 mL) and 1M sodium hydroxide solution (1 mL) were added to the reaction and stirred for 55 minutes. The solvents were then concentrated in vacuo. The residue was partitioned between chloroform (10 mL) and water (10 mL). The layers were separated and the aqueous was again extracted with chloroform. The combined organic layers were dried and concentrated in vacuo. The residue was purified using preparative TLC eluting with 1:1 acetone:cyclohexane to afford the title compound (41 mg 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409907B2
Source datasetuspto-grants-2016_08
ORD IDord-1bd467a0105f480c9c358eda5028cc35
Source noteuspto-grants-2016_08