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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466748Generated: October 31, 2026

Phenylglyoxylic Acid → HCID 57344122, compound

https://huagongshe.com/reaction/1466748

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylglyoxylic AcidHCID 11915—
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 57344122HCID 5734412242%

Reaction Steps

4-(3-(1,4-diazepane-1-carbonyl)-4-fluorobenzyl)phthalazin-1(2H)-one TFA salt (320 mg, 0.65 mmol), 2-oxo-2-phenylacetic acid (1.4 g, 9.32 mmol), DIPEA (3 ml, 17.4 mmol), and HATU (1.8 g, 4.72 mmol) were mixed in DMF (50 ml). After the resulting reaction mixture was stirred at room temperature for 85 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 preparative TLC (Petroleum ether:Ethyl Acetate=1:1 to 1:2) to afford the desired product (140 mg, 41%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999985B2
Source datasetuspto-grants-2015_04
ORD IDord-b620728fad5343d3b4609342841db454
Source noteuspto-grants-2015_04