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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480842Generated: November 2, 2026

Sodium hydride → HCID 89996303, compound

https://huagongshe.com/reaction/1480842

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 89996157HCID 89996157—
ReactantHCID 89996299HCID 89996299—
SolventTetrahydrofuranHCID 8028—
ProductHCID 89996303HCID 89996303121.1%

Reaction Steps

To a cooled (0° C.) suspension of N-(2-methyl-4-(1-methyl-1H-pyrazol-4-yl)phenyl)formamide (Preparation 99, 40 mg, 0.186 mmol) in THF (4 mL) was added NaH (60% dispersion in oil, 12 mg, 0.297 mmol). The reaction mixture was stirred at room temperature for 10 minutes. The reaction mixture was cooled to 0° C. and 8-chloro-2-(methylsulfonyl)pyrido[3,4-d]pyrimidine (Preparation 97, 59 mg, 0.242 mmol) was added. The reaction mixture was stirred for 18 hours, whilst slowly warming to room temperature. The reaction mixture was concentrated in vacuo. The residue was partitioned between EtOAc (30 mL) and water (30 mL). The aqueous layer was extracted with EtOAc (30 mL) and DCM (30 mL). The combined organic layers were washed with water (30 mL) and brine (30 mL), dried (MgSO4) and concentrated in vacuo. The residue was purified by silica gel column chromatography eluting with 0-5% MeOH in EtOAc to give the title compound (79 mg, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409907B2
Source datasetuspto-grants-2016_08
ORD IDord-4e2b4f11041d4625b1a1313e3572b111
Source noteuspto-grants-2016_08