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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52272Generated: October 28, 2026

Acetic Acid → (R)-3-(N-Cyclobutyl-N-n-propylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran

https://huagongshe.com/reaction/52272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPropanalHCID 527—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 53650127HCID 53650127—
SolventMethanolHCID 887—
Product(R)-3-(N-Cyclobutyl-N-n-propylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyranHCID 2287121880.6%

Reaction Steps

(R)-3-(N-Cyclobutylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran (1.01 g, 4.02 mmol) was dissolved in anhydrous methanol (20 mL) and to this was n-propionaldehyde (3.0 mL, 40.2 mmol) added. After 1 h the reaction was cooled (ice-bath) then sodium cyanoborohydride (0.46 g, 7.24 mmol) was added, the pH was adjusted to 4-5 with acetic acid and the reaction was allowed to stir at room temperature over the weekend. The solvent was removed in vacuo, the remains extracted thrice with diethyl ether. The combined ether portions were dried (MgSO4) filtered, and the solvent were taken into a 2M solution of NH3 and then removed in vacuo to give the crude residue. Chromatography on silica (eluent: 11% ethyl acetate/hexane) gave 0.95 g (80% yield) of the title compound as a clear oil. [α]21D =-95.4° (C=0.1; CHCl3) GC-MS (70 eV) M=293 (1%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616610
Source datasetuspto-grants-1997_04
ORD IDord-52880a17bb9b4f3d90dd1edb0f188ee1
Source noteuspto-grants-1997_04