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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1182125Generated: November 2, 2026

3,4,5-Trimethoxybenzoic Acid → N-{(S)-1-tert-butoxymethyl-3-[3-(4-fluoro-phenoxy)-azetidin-1-yl]-propyl}-3,4,5-trimethoxy-benzamide

https://huagongshe.com/reaction/1182125

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-Trimethoxybenzoic AcidHCID 8357—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-benzotriazol-1-yl-tetramethyluroniumHCID 130500—
Reactant(4,5-Bis-methoxycarbonyl-[1,3]dithiol-2-yl)-tributyl-phosphoniumHCID 498382—
Reactant(S)-1-tert-butoxymethyl-3-[3-(4-fluoro-phenoxy)-azetidin-1-yl]-propylamineHCID 69411039—
SolventDimethylformamideHCID 6228—
ProductN-{(S)-1-tert-butoxymethyl-3-[3-(4-fluoro-phenoxy)-azetidin-1-yl]-propyl}-3,4,5-trimethoxy-benzamideHCID 10289176—

Reaction Steps

A solution of 3,4,5-trimethoxy-benzoic acid (0.246 g, 1.16 mmol) and diisopropylethylamine (0.62 ml, 3.47 mmol) in dry dimethylformamide (10 ml) is treated with [(benzotriazol-1-yloxy)-dimethylamino methylene]-dimethyl-ammonium; tetrafluoro borate (0.32 g, 1.0 mmol). The reaction mixture is stirred at ambient temperature for 5 minutes, then (S)-1-tert-butoxymethyl-3-[3-(4-fluoro-phenoxy)-azetidin-1-yl]-propylamine (0.968 mmol) is added and the reaction mixture stirred for 20 hours. The dimethylformamide is evaporated and the residue partitioned between ethylacetate and saturated aqueous NaHCO3. The ethylacetate phase is washed with brine, dried over MgSO4 and evaporated. The crude product is purified by flash silica chromatography (elution 50% ethylacetate/hexane to 100% ethylacetate) to afford N-{(S)-1-tert-butoxymethyl-3-[3-(4-fluoro-phenoxy)-azetidin-1-yl]-propyl}-3,4,5-trimethoxy-benzamide [MH]+ 505.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07288537B2
Source datasetuspto-grants-2007_10
ORD IDord-d08c81c44dd54631bf1a2672cd96e0f7
Source noteuspto-grants-2007_10