Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727390Generated: November 4, 2026

Acetic Acid → 8-{[4-(5-fluoro-1H-indol-3-yl)butyl]amino}-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-one

https://huagongshe.com/reaction/1727390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant4-(5-fluoro-1H-indol-3-yl)butanalHCID 11846010—
Reactant8-amino-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-oneHCID 57567669—
SolventMethanolHCID 887—
Product8-{[4-(5-fluoro-1H-indol-3-yl)butyl]amino}-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-oneHCID 4622531078%

Reaction Steps

To a mixture of (1) (60 mg, 0.294 mmol), 4-(5-fluoro-1H-indol-3-yl)butanal (21), 63 mg, 0.294 mmol) in acetic acid (37 μl, 0.62 mmol) and methanol (4 ml) was added NaBH3CN (37 mg, 0.588 mmol) in portions. Resulting mixture was stirred for 1.5 hr. The solvent was removed in vacuo and the residue was dissolved in CH2Cl2 and washed with 1 N NaOH and saturated NaCl. The organic solution was dried over Na2SO4 and concentrated in vacuo. The compound was purified on silica gel eluting with 60% EtOAc/Hexane to give (25) as a solid (90 mg, 78%). MS (ES) m/z 394.2;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495111B2
Source datasetuspto-grants-2009_02
ORD IDord-5874ff6b482d4599ac6e679eaac3dbd0
Source noteuspto-grants-2009_02