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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2096031Generated: October 25, 2026

Sodium Bicarbonate → 1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamide

https://huagongshe.com/reaction/2096031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant2-bromo-1-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]ethanoneHCID 86631247—
ReactantN-(2,5-dimethylphenyl)-4-thiocarbamoylpiperidine-carboxamideHCID 86645615—
SolventAcetoneHCID 180—
Product1-[4-[4-[(5R)-4,5-dihydro-5-phenyl-3-isoxazolyl]-2-thiazolyl]-1-piperidinyl]-N-[2,5-dimethylphenyl]carboxamideHCID 131730596—

Reaction Conditions

Temperature45 °C

Reaction Steps

A mixture of N-(2,5-dimethylphenyl)-4-thiocarbamoylpiperidine carboxamide (i.e. the product of Example 14, Step B) (291 mg, 1.0 mmol) and 409 (i.e. the product of Example 12, Step E) (268 mg, 1.0 mmol) in acetone (10 mL) was vortexed for 16 h and then heated at 45° C. for 1 h. The reaction mixture was allowed to cool to room temperature, treated with solid sodium bicarbonate (168 mg, 2.0 mmol), and stirred for 1 h. The reaction mixture was then concentrated under reduced pressure, diluted with ethyl acetate, washed with water and brine, dried (MgSO4), and concentrated under reduced pressure to give the title product as a pale-yellow foam. The sample was dissolved in methyl acetate (2 mL) and allowed to sit at room temperature and then at 0° C. to give 220 mg of colorless crystals melting at 120-125° C. A second preparation was crystallized from methanol to give large prisms melting at 121-124° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08449898B2
Source datasetuspto-grants-2013_05
ORD IDord-0679f54b3ef04b44b9ff53f8b0578d78
Source noteuspto-grants-2013_05