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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025543Generated: November 1, 2026

Diisopropylethylamine → HCID 53245737, compound

https://huagongshe.com/reaction/1025543

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantDecahydroisoquinolineHCID 97812—
ReactantHCID 15015183HCID 15015183—
SolventTetrahydrofuranHCID 8028—
ProductHCID 53245737HCID 53245737—

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729098B2
Source datasetuspto-grants-2014_05
ORD IDord-69d750c087d14bb0b2df8de77f4f63a4
Source noteuspto-grants-2014_05