HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579185Generated: October 30, 2026
Hydrochloric Acid → HCID 66692147, compound
https://huagongshe.com/reaction/579185
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | Methanol tetrahydrofuran water | HCID 21892291 | — |
| Reactant | 3-((3S,6S)-6-Cyclohexyl-3-hydroxy-2-oxo-piperidin-1-yl)-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester | HCID 66684775 | — |
| Product | HCID 66692147 | HCID 66692147 | 57% |
Reaction Steps
To a solution of 3-((3S,6S)-6-Cyclohexyl-3-hydroxy-2-oxo-piperidin-1-yl)-5-(3,3-dimethyl-but-1-ynyl)-thiophene-2-carboxylic acid methyl ester (1.5 g, 3.59 mmol, 1 equiv.) in THF/H2O/MeOH (5.0 mL/5.0 mL/1.0 mL) was added LiOH.H2O (0.79 g, 17.56 mmol, 5.0 equiv.) at room temperature. The reaction mixture was stirred at 50° C. for 20 minutes. The reaction was then acidified to pH=5 by addition of 3.0 N HCl aq. solution and the mixture was extracted with EtOAc. The organic layer was dried over Na2SO4, and concentrated. The residue was purified by prep-HPLC (XBridge Prep C 18 5 um, 30×50 mm) in basic condition (0.1% NH4OH, 10%˜45% CH3CN/H2O, 10 min run, 40 ml/min) to give 850 mg of product (yield 57%). MS: 404 [M+H+]. 1H-NMR (400 MHz, MeOD): δ 6.95 (s, 1H), 4.09 (m, 1H), 3.74 (m, 1H), 2.09 (m, 1H), 1.94-1.67 (m, 8H), 1.38 (m, 1H), 1.33 (s, 9H), 1.17 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040690B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-bb5ab0c2f33c42238781db21826679b9 |
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| Source note | uspto-grants-2015_05 |
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