HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 625140Generated: October 30, 2026
Succinic anhydride → HCID 68281999, compound
https://huagongshe.com/reaction/625140
Participants
| Role | Name | HCID | Charge |
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| Reactant | Succinic anhydride | HCID 7922 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-Propanamine, 3-[(3b)-cholest-5-en-3-yloxy]- | HCID 57358590 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 68281999 | HCID 68281999 | 114.9% |
Reaction Steps
In a 2 μL round-bottomed flask, 3-((3S,8S,9S,10R,13R,14S,17R)-10,13-dimethyl-17-((R)-6-methylheptan-2-yl)-2,3,4,7,8,9,10,11,12,13,14,15,16,17-tetradecahydro-1H-cyclopenta[a]phenanthren-3-yloxy)propan-1-amine (21.15 g, 47.7 mmol, Eq: 1.00) and Huenig's base (12.3 g, 16.6 ml, 95.3 mmol, Eq: 2.00) were combined with AcOEt (845 ml) to give a colorless solution. Dihydrofuran-2,5-dione (4.77 g, 47.7 mmol, Eq: 1.00) in THF (42 ml) was added and the reaction mixture was stirred at ambient temperature over night=>white suspension. All volatiles were removed i. v., the residue dissolved in CH2Cl2, the organic layer washed with NH4Cl and brine, dried over Na2SO4, and evaporated to dryness. The crude product was dissolved in CH3CN/H2O and lyophilized to yield 29.8 g of the title compound as fluffy powder. MS (ISP): (M−H) 542.5.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09301990B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-3a5c173a2ce94c38b5e3f0d2ef5d7ab5 |
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| Source note | uspto-grants-2016_04 |
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