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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469710Generated: October 27, 2026

Hydrochloric Acid → HCID 67953841, compound

https://huagongshe.com/reaction/469710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,1-DichloroethaneHCID 6365—
ReactantSodium BisulfateHCID 516919—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant(S)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amideHCID 67455816—
CatalystAcetic AcidHCID 176—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
ProductHCID 67953841HCID 67953841—

Reaction Steps

A solution of acetone and (S)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide; hydrochloride (0.2 g; 0.843 mmol) in dichloroethane (3 mL) with several drops of acetic acid and approximately 10 equivalents of sodium bisulfate is stirred for 30 minutes followed by the addition of sodium cyanoborohydride (0.079 g; 1.265 mmol). The mixture is stirred overnight at room temperature. After this time, the mixture is diluted with ethyl acetate and washed with aqueous sodium bicarbonate solution and brine. The organics are dried (Na2SO4), filtered and concentrated in vacuo to afford crude material. Excess starting material is removed using polystryrene bound-isocyante resin (500 mg: 1.51 mmol/g) in dichloromethane (5 mL) for several hours. Crude product is eluted from resin using methylene chloride and tetrahydrofuran. The filtrate is concentrated and final purification done using reverse phase preparative HPLC to afford title compound. ESI m/z 280 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629157B2
Source datasetuspto-grants-2014_01
ORD IDord-ff13884286ce4e15a2e6585126a25bd7
Source noteuspto-grants-2014_01