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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1942728Generated: November 2, 2026

Acetic Acid → 1-{2-[3-{5-[3-Cyano-4-(2-methylpropyl)phenyl]-1,3,4-thiadiazol-2-yl}-5-fluoro-2-(methyloxy)phenyl]ethyl}-3-azetidinecarboxylic acid

https://huagongshe.com/reaction/1942728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-azetidinecarboxylic AcidHCID 93192—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant5-{5-[5-Fluoro-2-(methyloxy)-3-(2-oxoethyl)phenyl]-1,3,4-thiadiazol-2-yl}-2-(2-methylpropyl)benzonitrileHCID 86659003—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product1-{2-[3-{5-[3-Cyano-4-(2-methylpropyl)phenyl]-1,3,4-thiadiazol-2-yl}-5-fluoro-2-(methyloxy)phenyl]ethyl}-3-azetidinecarboxylic acidHCID 5457959021%

Reaction Steps

To a solution of 5-{5-[5-fluoro-2-(methyloxy)-3-(2-oxoethyl)phenyl]-1,3,4-thiadiazol-2-yl}-2-(2-methylpropyl)benzonitrile (D37) (75 mg) and 3-azetidinecarboxylic acid (37 mg) in dichloromethane (DCM) (15 mL) stirred at room temperature was added AcOH (0.15 mL). The reaction mixture was stirred at room temperature for 10 min. Then sodium triacetoxyborohydride (58.2 mg) was added. Stirring continued for overnight. Water was added to quench the reaction, and DCM was removed by evaporation. The mixture was extracted by EA/THF/MeCN for 3 times. The combined organic solution was washed by brine, dried over anhydrous Na2SO4. The dried solution was filtered and concentrated. The residue was purified by Mass Directed AutoPrep to give 1-{2-[3-{5-[3-cyano-4-(2-methylpropyl)phenyl]-1,3,4-thiadiazol-2-yl}-5-fluoro-2-(methyloxy)phenyl]ethyl}-3-azetidinecarboxylic acid (E15) (19 mg) as an off-white solid. δH (DMSO-d6, 400 MHz): 0.94 (6H, d), 1.99 (1H, m), 2.33 (1H, m), 2.67 (4H, m), 2.77 (2H, d), 3.17 (4H, m), 3.80 (3H, s), 7.47 (1H, dd), 7.68 (1H, d), 7.90 (1H, dd), 8.34 (1H, dd), 8.50 (1H, d). δF (DMSO-d6, 376 MHz): −117.2. MS (ES): C26H27FN4O3S requires 494. found 495.2 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08389508B2
Source datasetuspto-grants-2013_03
ORD IDord-e37e6fa77ff74be9b1e5e3de3886b7e5
Source noteuspto-grants-2013_03