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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1727391Generated: November 3, 2026

Acetic Acid → 8-{[(6-fluoro-2,3,4,9-tetrahydro-1H-carbazol-3-yl)methyl]amino}-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-one

https://huagongshe.com/reaction/1727391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant6-Fluoro-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehydeHCID 25139506—
Reactant8-amino-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-oneHCID 57567669—
SolventMethanolHCID 887—
Product8-{[(6-fluoro-2,3,4,9-tetrahydro-1H-carbazol-3-yl)methyl]amino}-2,3,8,9-tetrahydropyrano[3,2-e]isoindol-1(7H)-oneHCID 69061637—

Reaction Steps

To a mixture of (1) (60 mg, 0.294 mmol), 6-fluoro-2,3,4,9-tetrahydro-1H-carbazole-3-carbaldehyde ((28), 64 mg, 0.294 mmol) in acetic acid (38 mg, 0.588 mmol) and methanol (3 ml) was added NaBH3CN (37 mg, 0.588 mmol) in portions. The resulting mixture was stirred for 40 min. The solvent was removed in vacuo and the residue was dissolved in methylene chloride. The organic solution was washed with 1N NaOH and saturated NaCl before being dried over with Na2SO4. The concentration of organic solution in vacuo gave crude (27), which was purified on silica gel eluting with 80% EtOAc/Hexane to give a white solid (71 mg, 60%). MS (ES) m/z 406.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07495111B2
Source datasetuspto-grants-2009_02
ORD IDord-aab4cf6ab1cd4568ab4aaaca2bc25db0
Source noteuspto-grants-2009_02