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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727387Generated: November 2, 2026

Acetic Acid → 8-{[3-(5-fluoro-1H-indol-3-yl)propyl]amino}-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-one

https://huagongshe.com/reaction/1727387

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant3-(5-fluoro-1H-indol-3-yl)propanalHCID 11846179—
Reactant8-amino-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-oneHCID 57567669—
SolventMethanolHCID 887—
Product8-{[3-(5-fluoro-1H-indol-3-yl)propyl]amino}-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-oneHCID 1609210782%

Reaction Steps

To a solution of 8-amino-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-one (1) (200 mg, 0.98 mmol) in anhydrous MeOH (20 ml) was added 3-(5-fluoro-1H-indol-3-yl) propanal (2) (191 mg, 1 mmol), AcOH (0.14 ml), and NaBH3CN (123 mg, 1.96 mmol). Resulting reaction mixture was stirred at room temperature for 2 hr. The solvent was removed in vacuo and the residue was re-dissolved in CH2Cl2 (150 ml). The solution was washed with 1 N NaOH (20 ml) and H2O, Sat. NaCl. The organic solution was separated, dried over Na2SO4, then concentrated in vacuo. The crude compound was purified on silica gel eluting with EtOAc/Hexane (4:1) to yield (3) (304 mg, 82%) as a white solid. MS (APPI) m/z 380.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495111B2
Source datasetuspto-grants-2009_02
ORD IDord-d250162132a44b63ad0ba4ea44279f4e
Source noteuspto-grants-2009_02