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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1616415Generated: November 2, 2026

Acetic Acid → methyl 5-bromo-3-((cyclopropylmethyl)(tetrahydro-2H-pyran-4-yl)amino)-2-methylbenzoate

https://huagongshe.com/reaction/1616415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantCyclopropanecarboxaldehydeHCID 123114—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactantmethyl 5-bromo-2-methyl-3-((tetrahydro-2H-pyran-4-yl)amino)benzoateHCID 70872676—
SolventMethanolHCID 887—
Productmethyl 5-bromo-3-((cyclopropylmethyl)(tetrahydro-2H-pyran-4-yl)amino)-2-methylbenzoateHCID 7087267123.7%

Reaction Steps

To a stirred solution of methyl 5-bromo-2-methyl-3-((tetrahydro-2H-pyran-4-yl)amino)benzoate (1 g, 3.04 mmol) and cyclopropanecarbaldehyde (1.06 g, 15.24 mmol) in methanol (15 mL), acetic acid (0.456 g, 7.6 mmol) was added The reaction mixture was stirred at room temperature for 8 h. Sodium cyanoborohydride (0.488 g, 7.62 mmol) was then added at 0° C. and reaction mixture stirred overnight at room temperature. The solvent was then removed under reduced pressure and the crude product purified by column chromatography to afford methyl 5-bromo-3-((cyclopropylmethyl)(tetrahydro-2H-pyran-4-yl)amino)-2-methylbenzoate (0.275 g, 23.70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765732B2
Source datasetuspto-grants-2014_07
ORD IDord-5e21ec2a04694cabbbf5af5276edef23
Source noteuspto-grants-2014_07