Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Putrescine | HCID 1045 | — |
| Reactant | 5,6alpha-Epoxicholest-7-en-3beta-ol | HCID 87226647 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 44598468 | HCID 44598468 | 64% |
Reaction Steps
5,6α-epoxicholest-7-en-3β-ol (8.9 g, 22.1 mmol, 1 eq) and putrescine (3.9 g, 44.1 mmol, 2 eq) were charged in a round-bottomed flask equipped with a magnetic stirrer bar. 1-Butanol (70 ml, 5 vol) was added and the mixture heated to reflux for 40 h. The reaction mixture was cooled at r.t., diluted with methyl-tertbutyl-ether (5 vol) and washed with water (5 vol) and with brine (5 vol). The organic layer was passed through a silica pad (40 g) eluted with methyl-tertbutyl-ether (3 vol) then 10% Methanol/ethyl acetate (60 vol). Fractions of interest were pooled and the solvent was removed under reduced pressure to give 5α-Hydroxy-6β-(4-aminobutylamino)-cholest-7-en-3β-ol as a white solid (6.9 g, 64%). In same conditions, use of ethanol as solvent (40 vol) and Ca(OTf)2 as catalyst gave a 23% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447141B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-cb464e1b8192482d8e8159b75140705d |
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| Source note | uspto-grants-2016_09 |
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