HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1184115Generated: October 31, 2026
Sodium methanolate methanol → tert-butyl (3R,5S)-3-(1-hydroxy-2-methoxyethyl)-5-[{[1-(4-methoxybutyl)-1H-benzimidazol-2-yl]carbonyl}(2-methylpropyl)amino]piperidine-1-carboxylate
https://huagongshe.com/reaction/1184115
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium methanolate methanol | HCID 23694274 | — |
| Reactant | tert-Butyl (3S,5R)-3-[{[1-(4-methoxybutyl)-1H-benzimidazol-2-yl]carbonyl}(2-methylpropyl)amino]-5-oxirane-2-ylpiperidine-1-carboxylate | HCID 58355125 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | tert-butyl (3R,5S)-3-(1-hydroxy-2-methoxyethyl)-5-[{[1-(4-methoxybutyl)-1H-benzimidazol-2-yl]carbonyl}(2-methylpropyl)amino]piperidine-1-carboxylate | HCID 58355142 | — |
Reaction Steps
tert-Butyl (3S,5R)-3-[{[1-(4-methoxybutyl)-1H-benzimidazol-2-yl]carbonyl}(2-methylpropyl)amino]-5-oxirane-2-ylpiperidine-1-carboxylate (200 mg) was dissolved in methanol (5 ml), 28% sodium methylate-methanol solution was added, and the mixture was stirred at 70° C. for 6 hr. The solvent was evaporated under reduced pressure, and the residue was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (1:1-1:0) was concentrated under reduced pressure to give the object product (157 mg). MS (ESI+, m/e) 561(M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08664380B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-4d545112da954c5dbc163a40c278a577 |
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| Source note | uspto-grants-2014_03 |
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