HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469710Generated: October 27, 2026
Hydrochloric Acid → HCID 67953841, compound
https://huagongshe.com/reaction/469710
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (S)-pyrrolidine-2-carboxylic acid (5-tert-butyl-isoxazol-3-yl)-amide | HCID 67455816 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67953841 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08629157B2 |
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| Source dataset | uspto-grants-2014_01 |
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| ORD ID | ord-ff13884286ce4e15a2e6585126a25bd7 |
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| Source note | uspto-grants-2014_01 |
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