HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1893447Generated: October 31, 2026
3-Amino-1-propanol → HCID 59333332, compound
https://huagongshe.com/reaction/1893447
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Amino-1-propanol | HCID 9086 | — |
| Reactant | HCID 59333318 | HCID 59333318 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 59333332 | HCID 59333332 | 85.4% |
Reaction Steps
To a solution of 4-chloro-1-(4-methoxy-phenyl)-7-trifluoromethyl-1H-imidazo[4,5-c]quinoline (153 mg; 0.41 mmol; 1 eq) in anhydrous 1,4-dioxane (18 mL), 3-aminopropanol (77 μL; 1.0 mmol; 2.5 eq) is added. The resulting solution is heated to reflux and allowed to stir for 19 hours after which period the reaction is still not complete on TLC. Thus, additional 3-aminopropanol (523 μL; 6.9 mmol; 17 eq) is added and the stirring is continued under reflux for 4 hours. The crude mixture is diluted with ethyl acetate (40 mL) and washed three times with a 1M aqueous solution of NaOH (3×40 mL). Aqueous layers are combined and re-extracted with ethyl acetate (75 mL). All organic layers are combined, dried over sodium sulfate and concentrated. The crude residue is purified on silica gel (cyclohexane/ethyl acetate 2:8) to afford the title compound as an off-white powder (145 mg; 0.35 mmol; 85%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08513250B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-51962b4f82414514bc460af00481b48d |
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| Source note | uspto-grants-2013_08 |
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