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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466749Generated: October 29, 2026

2-Furylglyoxylic acid → HCID 57344123, compound

https://huagongshe.com/reaction/1466749

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Furylglyoxylic acidHCID 73846—
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 86693909HCID 86693909—
SolventDimethylformamideHCID 6228—
ProductHCID 57344123HCID 5734412334%

Reaction Steps

4-(3-(1,4-diazepane-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-one TFA salt (320 mg, 0.65 mmol), 2-(furan-2-yl)-2-oxoacetic acid (563 mg, 4 mmol), DIPEA (1 ml, 6 mmol), and HATU (510 mg, 1.34 mmol) were mixed in DMF (30 ml). After the resulting reaction mixture was stirred at room temperature for 60 h, the reaction mixture was partition between DCM and water (100 ml each). The aqueous phase was extracted with DCM (100 ml), and the combined organic phase was washed with water, sat. aqueous sodium bicarbonate, and brine, dried over sodium sulphate, filtered, and concentrated to yield the crude product. Then the crude product was purified by column chromatography on silica gel (Petroleum ether:Ethyl Acetate=1:3) to afford the desired product (111 mg, 31%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999985B2
Source datasetuspto-grants-2015_04
ORD IDord-459960b72fcc4a5aa0cc2796ea9d27f7
Source noteuspto-grants-2015_04