HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272234Generated: October 30, 2026
Hydrochloric Acid → HCID 178468875, compound
https://huagongshe.com/reaction/272234
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-benzyloxy-3-(N-tert-butoxycarbonyl-N-methylsulfonylamino)-1-((2S)-2,3-epoxypropoxy)benzene | HCID 11201748 | — |
| Reactant | HCID 178468874 | HCID 178468874 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178468875 | HCID 178468875 | — |
Reaction Steps
A mixture of 818 mg (1.82 mmol) of 4-benzyloxy-3-(N-(tert-butoxycarbonyl)-N-(methylsulfonyl)amino)-1-((2S)-2,3-epoxypropoxy)benzene and of 450 mg (1.82 mmol) of ethyl trans-4-[4-(benzylamino)cyclohexyl]benzoate in the base form is heated at reflux in 15 ml of absolute ethanol for 16 h. The mixture is cooled, 3 ml of a saturated ethanolic hydrochloric acid solution are added thereto and the mixture is heated at 50° C. for 6 h. The solvent is evaporated and the residue is taken up with a mixture of 50 ml of a saturated sodium bicarbonate solution and 50 ml of ethyl acetate. The organic phase is washed with a saturated aqueous NaCl solution. The organic phase is dried and filtered, and the solvent is evaporated under reduced pressure. The crude product is purified by chromatography on a column of silica gel, elution being carried out with a methylene chloride/methanol/NH4OH (95/5/0.5) mixture. The title compound is obtained in the form of a white solid. [M+H+]=687.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07453010B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-668bcdfc7ef0422aa9220bb6c9e0f320 |
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| Source note | uspto-grants-2008_11 |
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