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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1245384Generated: October 27, 2026

Diisopropylethylamine → N-Hydroxy-2-{3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-4,5-dihydro-isoxazol-5-yl}-acetamide

https://huagongshe.com/reaction/1245384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHydroxyamine hydrochlorideHCID 443297—
Reactant{3-[4-(2-Methyl-quinolin-4-ylmethoxy)-phenyl]-4,5-dihydro-isoxazol-5-yl}-acetic acidHCID 21911127—
SolventDimethylformamideHCID 6228—
ProductN-Hydroxy-2-{3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-4,5-dihydro-isoxazol-5-yl}-acetamideHCID 986524031.9%

Reaction Steps

The {3-[4-(2-methyl-quinolin-4-ylmethoxy)-phenyl]-4,5-dihydro-isoxazol-5-yl}-acetic acid (0.15 g, 0.4 mmol) was combined with BOP (0.265 g, 0.6 mmol) and diisopropylethylamine (0.5 mL) in DMF (5 mL) under nitrogen atmosphere at room temperature. The reaction was stirred for 15 minutes, and then hydroxylamine hydrochloride (0.042 g, 0.6 mmol) was added. The reaction was stirred overnight, concentrated in vacuo, and triturated with water saturated KH2PO4 solution to give a precipitate. The crude product was purified by HPLC on a C-18 column eluting with an acetonitrile/water/TFA gradient to give the title compound (0.05 g, 25%) as an amorphous solid. MS found: (M+H)+=392.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07125870B2
Source datasetuspto-grants-2006_10
ORD IDord-6ccbc202c1134e9a856dc8b5b8076f2b
Source noteuspto-grants-2006_10