HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466748Generated: October 31, 2026
Phenylglyoxylic Acid → HCID 57344122, compound
https://huagongshe.com/reaction/1466748
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phenylglyoxylic Acid | HCID 11915 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Reactant | HCID 86693909 | HCID 86693909 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57344122 | HCID 57344122 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08999985B2 |
|---|
| Source dataset | uspto-grants-2015_04 |
|---|
| ORD ID | ord-b620728fad5343d3b4609342841db454 |
|---|
| Source note | uspto-grants-2015_04 |
|---|