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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1445115Generated: November 1, 2026

Water → HCID 67142101, compound

https://huagongshe.com/reaction/1445115

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenemethanamine, 3-chloro-HCID 77802—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86615265HCID 86615265—
CatalystTitanium isopropoxideHCID 11026—
SolventMethanolHCID 887—
ProductHCID 67142101HCID 6714210157.5%

Reaction Steps

A solution of 7-(3,4-dihydro-1H-isoquinolin-2-yl)-1-(3-fluorobenzyl)-2,3-dimethyl-1H-pyrrolo[2,3-c]pyridin-5-carbaldehyde (30 mg, 0.07 mmol) prepared in Step 1 of Example 864 and 3-chlorobenzylamine (9.75 μl, 0.08 mmol) in methanol (3 ml) was refluxed for 3 hours. Titanium(IV) isopropoxide (40 μl) and sodium borohydride (5.49 mg, 0.15 mmol) were added at room temperature to the reaction mixture, which was then stirred overnight. Water was added to the reaction mixture, which was extracted with ethyl acetate. The organic layer was dried on anhydrous magnesium sulfate and then concentrated under reduced pressure. The resulting residue was purified with silica gel column chromatography (ethyl acetate/n-hexane=1/5, v/v) to give 21.7 mg of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662832B2
Source datasetuspto-grants-2010_02
ORD IDord-c0cfdb51f0b740a6b8fa8387e512db43
Source noteuspto-grants-2010_02