Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389834Generated: November 1, 2026

Acetic Acid → HCID 59313084, compound

https://huagongshe.com/reaction/2389834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium hydrideHCID 24758—
ReactantHCID 22142587HCID 22142587—
ReactantHCID 59312932HCID 59312932—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 59313084HCID 59313084—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-[(6-Amino-5-nitropyridin-2-yl)amino]ethanol (Example 48A) is introduced into DMF (3 ml) at 0° C., and sodium hydride (60% oil dispersion, 15 mg, 0.4 mmol) is added. The mixture is stirred at 0° C. for 10 min. 5-Chloro-7-(2,4-dichlorophenyl)imidazo[1,2-c]pyrimidine (Example 6A) (125 mg, 0.4 mmol) in DMF (1 ml) is added dropwise, and the reaction mixture is stirred at RT for 12 h. Glacial acetic acid (200 μl) is added, and the reaction mixture is poured into water and extracted with ethyl acetate (3×50 ml). The combined organic phases are washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate and concentrated. The residue is precipitated from acetonitrile, filtered off, washed with acetonitrile and dried. 36 mg (18% of theory) of product are obtained as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273752B2
Source datasetuspto-grants-2012_09
ORD IDord-be21db467c964ef38f6b1027d6e085cb
Source noteuspto-grants-2012_09