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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386912Generated: October 31, 2026

4-Methoxybenzylamine → HCID 59253151, compound

https://huagongshe.com/reaction/386912

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxybenzylamineHCID 75452—
ReactantTriacetoxyborohydrideHCID 2724942—
ReactantHCID 59253148HCID 59253148—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59253151HCID 5925315183%

Reaction Steps

To a solution of N-[3-(1,1-dimethyl-2-oxo-ethyl)-isoxazol-5-yl]-2-methyl-2-(tetrahydro-pyran-4-sulfonyl)-propionamide (130 mg, 0.35 mmol) in THF (2 mL) is added 4-methoxybenzylamine (0.055 mL, 0.42 mmol) and 2.7 mmol/g of MP-triacetoxyborohydride (323 mg, 0.87 mmol). The reaction mixture is placed on a shaker for 18 h. After this time, the reaction mixture is filtered and the filtrate is concentrated under reduced pressure. Purification by flash chromatography on silica gel using methanol/DCM provides the title compound. Yield: 83%; LC-MS retention time: 1.23 mins. ESI+ion mode. Zorbax SB-C18 column (3.5 μm, 4.6×30 mm). Gradient: 5% B to 80% B (0 min to 1.7 mins), 80% B to 95% B (1.7 mins to 2 mins), 95% B to 95% B (2 mins to 2.1 mins). Flow rate: 2.5 mL/min. A=(Water+0.1% Formic Acid) B=(Acetonitrile+0.1% Formic Acid). Diode Array Detector; m/z 494 [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372874B2
Source datasetuspto-grants-2013_02
ORD IDord-5ad1d50847af47a7b9cd3ee86afaedb6
Source noteuspto-grants-2013_02