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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 853763Generated: October 30, 2026

Sodium hydride → HCID 24856780, compound

https://huagongshe.com/reaction/853763

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2-Bromo-N-methylacetamideHCID 15490745—
ReactantHCID 24857371HCID 24857371—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 24856780HCID 2485678038%

Reaction Steps

Sodium hydride (60% in oil, 0.010 g, 0.25 mmol) is added to a solution of [2-(2,6-difluorophenoxy)-9-ethyl-9H-purin-8-yl]-(2-chlorophenyl)-amine, 14, (0.1 g, 0.25 mmol) in THF (3 mL). After 5 minutes at room temperature 2-bromo-N-methyl-acetamide (0.06 mL, 0.37 mmol) is added and stirring is continued for 1 hour. The mixture is diluted with H2O (25 mL) and extracted three times with EtOAc (50 mL). The combined organic layers are washed with brine, dried over MgSO4, concentrated in vacuo and the residue purified by HPLC to afford 45 mg (38% yield) of the desired product as a yellow solid. 1H NMR (300 MHz, CDCl3) δ 8.54 (s, 1H), 7.54-7.59 (m, 2H), 7.15-7.36 (m, 4H), 7.04 (t, J=7.8 Hz, 2H), 4.53 (s, 2H), 3.61 (q, J=7.2 Hz, 2H), 2.85 (d, J=4.8 Hz, 3H), 0.99 (t, J=7.2 Hz, 3H); ESI/MS: 473 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256196B1
Source datasetuspto-grants-2007_08
ORD IDord-f45bafcb7af646fe9c1ac475cd70a6a0
Source noteuspto-grants-2007_08