HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025543Generated: November 1, 2026
Diisopropylethylamine → HCID 53245737, compound
https://huagongshe.com/reaction/1025543
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Decahydroisoquinoline | HCID 97812 | — |
| Reactant | HCID 15015183 | HCID 15015183 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53245737 | HCID 53245737 | — |
Reaction Steps
A solution of 8-hydroxyquinoline-7-carbonyl chloride of Preparation 2 (70 mg, 0.35 mmol) and decahydroisoquinoline (62.6 mg, 0.45 mmol) in THF (8 mL) and DIPEA (259 mg, 2.0 mmol) was stirred and heated at 50° C. overnight. The reaction mixture was concentrated under reduced pressure and the residue was partitioned between DCM and H2O. The separated organics were dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography (silica gel, DCM:MeOH 98:2) and then by preparative HPLC. Product-containing fractions were combined, made basic with a saturated aqueous solution of sodium hydrogen carbonate and CH3CN was removed under reduced pressure. The aqueous phase was extracted with DCM and the separated organics dried over Na2SO4, filtered and concentrated to dryness, affording the title compound (49 mg, 0.16 mmol) as a off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729098B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-69d750c087d14bb0b2df8de77f4f63a4 |
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| Source note | uspto-grants-2014_05 |
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