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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942591Generated: October 26, 2026

Acetic Acid → HCID 58494145, compound

https://huagongshe.com/reaction/1942591

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium AcetateHCID 517045—
ReactantMethyl (azetidin-3-yl)acetateHCID 53408531—
Reactant3-(5-{3-Chloro-4-[(1-methylethyl)oxy]phenyl}-1,3,4-thiadiazol-2-yl)-2-ethylbenzaldehydeHCID 58494009—
SolventMethanolHCID 887—
ProductHCID 58494145HCID 58494145—

Reaction Steps

To a solution of 3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3,4-thiadiazol-2-yl)-2-ethylbenzaldehyde (D11) (43 mg) and methyl 3-azetidinylacetate (92 mg) in methanol (10.00 mL) stirred at room temperature was added sodium acetate (45.6 mg) and AcOH (0.032 mL). The reaction mixture was stirred at room temperature for 10 min. Then the solvent was removed by evaporation. The residue was dissolved in dichloromethane (DCM) (10 mL), and sodium triacetoxyborohydride (70.7 mg) was added. Stirring continued for 2 h. Water was added to quench the reaction, and DCM was removed by evaporation. The mixture was extracted by EA 3 times. The combined organic solution was washed by brine, dried over anhydrous Na2SO4. The dried solution was filtered and concentrated to give crude methyl 1-{[3-(5-{3-chloro-4-[(1-methylethyl)oxy]phenyl}-1,3,4-thiadiazol-2-yl)-2-ethylphenyl]methyl}-3-azetidinecarboxylate (D13) (54 mg). MS (ES): C25H28ClN3O3S requires 485. found 486.0 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389508B2
Source datasetuspto-grants-2013_03
ORD IDord-038096f84c8c4f06a92861507b5817a1
Source noteuspto-grants-2013_03