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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506263Generated: October 30, 2026

Cyanoacetic acid → HCID 71264074, compound

https://huagongshe.com/reaction/1506263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
ReactantHCID 71258513HCID 71258513—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventChloroform methanolHCID 21584188—
ProductHCID 71264074HCID 7126407411.4%

Reaction Steps

rac-1-[(3R,4R)-4-Methylpiperidin-3-yl]-1,2,4,7-tetrahydropyrrolo[3′,2′:5,6]pyrido[4,3-d][1,3]oxazine (21.2 mg, 0.0777 mmol) in N,N-dimethylformamide was stirred with cyanoacetic acid (15 mg, 0.18 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (67 mg, 0.18 mmol), N,N-diisopropylethylamine (44.9 μL, 0.264 mmol) at room temperature for one day. After addition of water, the reaction mixture was extracted with ethyl acetate, and the organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (Hi Flash column amino type manufactured by Yamazen Corporation: chloroform/methanol=20/1 (v/v)) to give the title compound as a yellow oil (3 mg, yield 10%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-be334cf04f2c4e2a97e195b83c8ddc6b
Source noteuspto-grants-2015_12