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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942111Generated: October 25, 2026

Dimethylformamide → 2-(1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-yl)-N-(4-isopropylphenyl)-N-methylacetamide

https://huagongshe.com/reaction/1942111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantAcefyllineHCID 69550—
ReactantAniline, p-isopropyl-N-methyl-HCID 138880—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
Product2-(1,3-dimethyl-2,6-dioxo-1,2,3,6-tetrahydropurin-7-yl)-N-(4-isopropylphenyl)-N-methylacetamideHCID 5920510884.4%

Reaction Steps

To a solution of acid 101 (0.5 g, 2.1 mmol) in CHCl3 (30 mL) and CH3CN (30 mL) at 0° C. was added oxalyl chloride (1.59 g, 12.6 mmol) and a catalytic amount of DMF. The resulting solution was stirred for 2 h at rt and concentrated in vacuo. The resulting residue was re-dissolved in CHCl3 and cooled to 0° C. To this mixture was added N-methyl-4-isopropyl aniline (0.78 g, 5.2 mmol) and the reaction was stirred overnight warming to rt. The reaction mixture was diluted with CHCl3 (30 mL) and washed with 1 N HCl (50 mL). The combined organic layers were washed with water (75 mL), dried over Na2SO4 and concentrated in vacuo. The product was purified by chromatography on silica gel eluting with EtOAc/hexanes and EtOAc/MeOH to yield 393 as a light yellow solid (0.65 g, 84.4%). mp: 231-233° C. MS (APCI): m/z 370.2 [M+H]+. Anal. Calcd. For C19H23N5O3.0.1 H2O: C, 61.47; H, 6.30; N, 18.87; Found C, 61.28; H, 6.19; N, 18.57.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389529B2
Source datasetuspto-grants-2013_03
ORD IDord-6a9db4f9225844bb8d749d2b90595256
Source noteuspto-grants-2013_03