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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237628Generated: October 30, 2026

Dimethylformamide → HCID 178511071, compound

https://huagongshe.com/reaction/2237628

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 178513913HCID 178513913—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178511071HCID 178511071—

Reaction Steps

To a stirred slurry of 2-{trans-4-[4-(4-amino-5-oxo-7,8-dihydropyrimido[5,4-f][1,4]oxazepin-6(5H)-yl)phenyl]cyclohexyl}acetamide (45 mg, 0.11 mmol), from Example 30, in THF (1 mL) was added DMF (0.002 mL) and oxalyl chloride (0.05 mL, 0.6 mmol). After two hours of stirring at room temperature, the reaction was quenched with aqueous sodium bicarbonate and extracted with EtOAc. The organic layer was washed with water, dried over sodium sulfate and concentrated in vacuo to afford the title compound as a light-yellow colored solid, 34 mg. 1H NMR (400 MHz, DMSO-d6): δ 8.17 (s, 1H), 7.63 (br s, 2H) 7.22 (m, 4H), 4.57 (m, 2H), 3.90 (m, 2H), 2.43 (m, 3H), 1.78 (m, 4H), 1.63 (m, 1H), 1.43 (m, 2H), 1.08 (m, 2H). m/z=378.3 (M+1). IC50 64.3 nM (range 51.2-91.1 nM).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718645B2
Source datasetuspto-grants-2010_05
ORD IDord-71f421057a93497bac5947527665fa69
Source noteuspto-grants-2010_05