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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404710Generated: October 27, 2026

Sodium Acetate → (4E)-4-methoxyimino-N-methyl-N-(5-pyridin-3-yl-1,3,4-thiadiazol-2-yl)pentanamide

https://huagongshe.com/reaction/1404710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
ReactantO-Methylhydroxylamine hydrochlorideHCID 521874—
ReactantN-methyl-4-oxo-N-[5-(3-pyridyl)-1,3,4-thiadiazol-2-yl]pentanamideHCID 66613626—
SolventEthanolHCID 702—
Product(4E)-4-methoxyimino-N-methyl-N-(5-pyridin-3-yl-1,3,4-thiadiazol-2-yl)pentanamideHCID 7333262337.1%

Reaction Steps

4-[(E)-methoxyimino]-pentanoic acid methyl-(5-pyridin-3-yl-[1,3,4]thiadiazol-2-yl)-amide was prepared as described in J F W Keana et al. in J. Org. Chem., 1985, 50, 2346. A suspension of O-methylhydroxylamine hydrochloride (0.065 g, 0.9 mmol), 4-oxo-pentanoic acid methyl-(5-pyridin-3-yl-[1,3,4]thiadiazol-2-yl)-amide (0.18 g, 0.6 mmol) and sodium acetate (0.076 g, 0.9 mmol) in anhydrous ethanol was refluxed under nitrogen for 14 hours, cooled, concentrated under reduced pressure and chromatographed on silica to afford the title compound as an amorphous yellow solid (0.071 g, 36%): mp 114-121° C.; 1H NMR (400 MHz, CDCl3) δ 9.15 (d, J=1.8 Hz, 1H), 8.70 (dd, J=4.8, 1.8 Hz, 1H), 8.29 (dt, J=5.9, 1.8 Hz, 1H), 7.43 (dd, J=7.7, 5.2 Hz, 1H), 3.92 (s, 3H), 3.86, 3.83 and 3.77 (all s, 1H), 2.95 (q, J=7.0 Hz, 2H), 2.71 (q, J=7.4 Hz, 2H), 2.11, 1.98 and 1.89 (all s, 3H); ESIMS m/z 320 ([M+H]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912338B2
Source datasetuspto-grants-2014_12
ORD IDord-c3dbcae2fb644b3d9f51795f44c77d04
Source noteuspto-grants-2014_12