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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361717Generated: October 27, 2026

Methyl 4-amino-2,5-dimethylbenzoate → Methyl 4-{3-[4-(biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionylamino}-2,5-dimethylbenzoate

https://huagongshe.com/reaction/1361717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-amino-2,5-dimethylbenzoateHCID 273299—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant3-[4-(Biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionic AcidHCID 21880607—
SolventDichloromethaneHCID 6344—
SolventDiisopropylethylamineHCID 81531—
ProductMethyl 4-{3-[4-(biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionylamino}-2,5-dimethylbenzoateHCID 4623962159%

Reaction Steps

To a stirred solution of 3-[4-(biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionic acid (670 mg, 1.82 mmol) and methyl 4-amino-2,5-dimethylbenzoate (390 mg, 2.18 mmol) in dichloromethane (3.6 mL) and diisopropylethylamine (0.413 mL) was added O-(7-azabenzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate (HATU) (829 mg, 2.18 mmol). The resulting mixture was stirred at room temperature overnight. The mixture was then washed with saturated aqueous sodium bicarbonate, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography eluting with dichloromethane containing from 3% to 5% methanol to provide methyl 4-{3-[4-(biphenyl-2-ylcarbamoyloxy)piperidin-1-yl]propionylamino}-2,5-dimethylbenzoate (568 mg, 59% yield). LCMS (10-70) Rt=4.55; [M+H+] found 530.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880010B2
Source datasetuspto-grants-2011_02
ORD IDord-29a67751b87441d08b777f0fb06f8f2f
Source noteuspto-grants-2011_02