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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948177Generated: November 2, 2026

4-Formylbenzoic acid → HCID 59340335, compound

https://huagongshe.com/reaction/1948177

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Formylbenzoic acidHCID 12088—
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—
ReactantBiphenyl-2-ylcarbamic acid 1-(2-aminoethyl)piperidin-4-yl esterHCID 53319786—
SolventDichloromethaneHCID 6344—
ProductHCID 59340335HCID 5934033592.2%

Reaction Steps

A mixture of 4-carboxybenzaldehyde (0.95 g, 6.35 mmol) and HATU (3.02 g, 7.94 mmol) in 55 mL of DCM was stirred at room temperature for 1 hour and then biphenyl-2-ylcarbamic acid 1-(2-aminoethyl)piperidin-4-yl ester (3 g, 5.29 mmol; prepared as described in Preparation 7) and DIPEA (4.6 mL, 26.45 mmol) were added. The resulting mixture was stirred at room temperature for 2 hours and then diluted with 100 mL of DCM and washed with saturated sodium bicarbonate (150 mL) and brine (150 mL). The organic layer was dried over MgSO4, filtered and concentrated to provide 2.3 g of the title intermediate (92% yield), which was suitable for use without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399488B2
Source datasetuspto-grants-2013_03
ORD IDord-7ebb92812fde48a19bd1b1ddbf7d6b82
Source noteuspto-grants-2013_03