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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 990389Generated: October 31, 2026

Benzyltrimethylammonium methoxide → HCID 23388389, compound

https://huagongshe.com/reaction/990389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyltrimethylammonium methoxideHCID 8504—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 12837668HCID 12837668—
ReactantHCID 13530069HCID 13530069—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 23388389HCID 2338838938.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of 291 mg (1.68 mmol) (S)-2-sec-butylamino-3-methyl-butyric acid, 500 mg (1.68 mmol) 4,4-bis-(4-fluoro-phenyl)-butylamine, 0.29 mL (1.68 mmol) N,N-diisopropylethylamine, and 1.5 mL (3.36 mmol) benzyltrimethylammonium methoxide (40% solution in methanol) in 4 mL dry DMF was cooled to 3° C. and 637 mg (1.68 mmol) O-Benzotriazol-1-yl-N,N,N′,N′-bis(tetramethylene)uronium hexafluorophosphate was added and the resulting mixture stirred at 3° for 30 minutes, warmed to 25° C., and stirred an additional 30 minutes at which time it was diluted with 20 mL diethyl ether, and washed with 20 mL saturated aqueous sodiumbicarbonate solution and twice with 20 mL brine, dried over anhydrous sodium sulfate and concentrated at reduced pressure. The residue thus obtained was further purified by silica gel chromatography using 70% ethyl acetate/hexanes as eluant, followed by conversion to the hydrochloride salt by treating with excess diethyl ether which had been saturated with hydrogen chloride gas to give 270 mg (35%) of titled compound: mp 77-81° C. APCI-MS m/z417.4 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458781B1
Source datasetuspto-grants-2002_10
ORD IDord-b8559fb2cad546128d29a7cf232f46e3
Source noteuspto-grants-2002_10