HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416013Generated: October 30, 2026
Hydrochloric Acid → HCID 57741545, compound
https://huagongshe.com/reaction/416013
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium cyanate | HCID 11378442 | — |
| Reactant | HCID 66622263 | HCID 66622263 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57741545 | HCID 57741545 | 46.4% |
Reaction Steps
Dissolve racemic 4-[3′,5′-dichloro-4′-(1-cyclohexyl-2-oxo-pyrrolidin-3-ylmethyl)-biphenyl-4-carbonyl]-piperazine-1-carboxylic acid tert-butyl ester (0.40, 0.65 mmol) in dioxane (20 mL), add 4N hydrochloric acid in dioxane (10 mL) and stir 30 min to obtain an orange residue in reaction vessel. Concentrate under vacuum, dilute residue with water (10 mL) and add potassium cyanate (0.55 g, 0.68 mmol). Stir the reaction at room temperature to obtain a white precipitate. Filter off solid and wash with water. Dissolve the solid in dichloromethane and concentrate under vacuum to yield a clear foam. Use resin bound solid phase acidic media (SCX) to remove residual starting material and obtain 0.168 g (46%) of product as a white solid: MS (m/z): 557 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08088776B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-48fce9ea3d7a4813a0f9f73157894abc |
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| Source note | uspto-grants-2012_01 |
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