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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530130Generated: October 30, 2026

Potassium Phosphate, Tribasic → 7-chloro-2-methyl-1-(3-methylbutyl)-1,4-dihydropyrido[3,4-b]pyrazin-3(2H)-one

https://huagongshe.com/reaction/530130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantN-(4,6-dichloropyridin-3-yl)-N2-(3-methylbutyl)alaninamideHCID 131735638—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product7-chloro-2-methyl-1-(3-methylbutyl)-1,4-dihydropyrido[3,4-b]pyrazin-3(2H)-oneHCID 8957040333%

Reaction Conditions

Temperature125 °C

Reaction Steps

To a stirred solution of N-(4,6-dichloropyridin-3-yl)-N2-(3-methylbutyl)alaninamide (350 mg, 1.15 mmol) in DMF (1.0 mL) was added tri-basic potassium phosphate (250 mg, 1.20 mmol). The reaction mixture was heated to 125° C. and stirred at the same temperature for 3 h. The reaction was then cooled to rt, diluted with water (5 mL) and the aqueous phase was extracted with ethyl acetate (25 mL×3). The combined organic phases were washed with water, dried over Na2SO4 and evaporated to give desired product (Yield: 33%), which was used for next step without any further purifications. 1HNMR (CDCl3, 300 MHz) δ 0.90-1.01 (m, 6H), 1.33 (d, 3H), 1.52-1.75 (m, 2H), 1.80 (s, 1H), 3.10-3.19 (m, 1H), 3.31-3.42 (m, 1H), 4.07 (q, 1H), 6.51 (s, 1H), 7.65 (s, 1H), 9.41 (br s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09351974B2
Source datasetuspto-grants-2016_05
ORD IDord-47de49c990d74351951366bdcf353e76
Source noteuspto-grants-2016_05