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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2301396Generated: October 30, 2026

Diisopropylethylamine → 3-{4-[(7-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-butyl}-[1,3]oxazinan-2-one

https://huagongshe.com/reaction/2301396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant7-methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amineHCID 10082172—
Reactant4-(2-Oxo-[1,3]oxazinan-3-yl)butyraldehydeHCID 15922696—
Solvent1,2-DichloroethaneHCID 11—
Product3-{4-[(7-Methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-butyl}-[1,3]oxazinan-2-oneHCID 15922697—

Reaction Steps

To (7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amine (ca. 13 mg 50 umole), was added 440 μL solution of 4-(2-oxo-[1,3]oxazinan-3-yl)-butyraldehyde (0.125 M in 1,2 dichloroethane), 30 μL diisopropylethylamine (DIEA) and 300 μL of 0.25 M slurry of sodium triacetoxyborohydride in 1,2 dichloroethane. The reaction was shaken at room temperature for 48 h. After quenching with 2 mL 2% NaOH, the reaction mixture was transferred along with 0.5 mL water and ethyl acetate to workup flasks. The organic phase was washed, dried and concentrated. Purification by chromatography yielded 3-{4-[(7-methoxy-1,2,3,4-tetrahydro-naphthalen-2-yl)-propyl-amino]-butyl}-[1,3]oxazinan-2-one 19, MS: 375 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06500822B2
Source datasetuspto-grants-2002_12
ORD IDord-7f93c167f8834b718aaeda04e658eaf7
Source noteuspto-grants-2002_12