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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298882Generated: November 1, 2026

1-Butanol → HCID 18378948, compound

https://huagongshe.com/reaction/2298882

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Chloro-1,2-benzisothiazoleHCID 598190—
ReactantHCID 18378946HCID 18378946—
SolventDichloromethaneHCID 6344—
ProductHCID 18378948HCID 18378948125.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 3,4-dihydro-7-methoxybenzofuro[2,3-c]pyridine-2(1H)-butanamine (0.0055 mol), 3-chloro-1,2-benzisothiazole (0.0089 mol) and NaHCO3 (0.01 mol) was stirred for 1.5 hour at 120° C. (melt). 1-Butanol (0.5 ml) was added. The reaction mixture was cooled, then dissolved in CH2Cl2 and purified by column chromatography over silica gel (eluent: CH2Cl2/(CH3OH/NH3) 98/2). The desired fractions were collected and the solvent was evaporated. The residue was dissolved in 2-propanone and converted into the hydrochloric acid salt (1:2) with HCl/2-propanol. The mixture was stirred at room temperature. The precipitate was filtered off and dried, yielding 1.60 g of N-(1,2-benzisothiazol-3-yl)-3,4-dihydro-7-methoxybenzofuro[2,3-c]pyridine-2(1H)-butanamine monohydrochloride monohydrate (61%) (compound 55).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495555B1
Source datasetuspto-grants-2002_12
ORD IDord-f44d742ea6364e92b9d6f15a652a66f8
Source noteuspto-grants-2002_12