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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1593649Generated: November 3, 2026

Acetic Acid → 1-(8-fluoro-1,2,3,4-tetrahydrodibenzo[b,d]furan-2-yl)-N-{[(2S)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl]methanamine

https://huagongshe.com/reaction/1593649

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant[(2S)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methylamineHCID 23521566—
Reactant8-Fluoro-1,2,3,4-tetrahydrodibenzo[b,d]furan-2-carbaldehydeHCID 86607649—
SolventMethanolHCID 887—
Product1-(8-fluoro-1,2,3,4-tetrahydrodibenzo[b,d]furan-2-yl)-N-{[(2S)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methyl]methanamineHCID 69235689—

Reaction Steps

8-fluoro-1,2,3,4-tetrahydrodibenzo[b,d]furan-2-carbaldehyde (0.040 g, 0.18 mmol), [(2S)-8-methyl-2,3-dihydro[1,4]dioxino[2,3-f]quinolin-2-yl]methylamine (0.042 g, 0.18 mmol), and NaBH3CN (0.023 g, 0.38 mmol) were stirred together in MeOH (1.2 mL) under a N2 atmosphere. To this mixture was added AcOH (0.023 mL) and reaction was allowed to stir for 3 h. The reaction mixture was concentrated and the resulting oil was purified by flash chromatography on silica gel to afford title compound as a mixture of two diastereomers (0.068 g, 88%). The diastereomers were separated by HPLC on a Chiracel AD column (2×25 cm), eluting with 100% ethanol; MS (ES) m/z=433.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07297704B2
Source datasetuspto-grants-2007_11
ORD IDord-c673d927c2aa4e0fb9dd2c0ae99c5866
Source noteuspto-grants-2007_11