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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098157Generated: November 1, 2026

(Isocyanoimino)triphenylphosphorane → N-(2-(1,3,4-oxadiazol-2-yl)thiophen-3-yl)-2-(naphthalen-1-yl)acetamide

https://huagongshe.com/reaction/2098157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Isocyanoimino)triphenylphosphoraneHCID 11266621—
Reactant3-(2-(Naphthalen-1-yl)acetamido)thiophene-2-carboxylic acidHCID 68755623—
SolventDichloromethaneHCID 6344—
ProductN-(2-(1,3,4-oxadiazol-2-yl)thiophen-3-yl)-2-(naphthalen-1-yl)acetamideHCID 4686907112.3%

Reaction Steps

To a solution of (isocyanoimino)triphenylphosphorane (978 mg, 3.24 mmol) in anhydrous CH2Cl2 (30 mL) was added dropwise a solution of 3-(2-(naphthalen-1-yl)acetamido)thiophene-2-carboxylic acid (340 mg, 1.09 mmol) in anhydrous CH2Cl2 (27 mL). The resulting mixture was stirred at room temperature under nitrogen overnight and evaporated under reduced pressure. Purification by flash chromatography (silica, 30:70 ethyl acetate/hexane) gave N-(2-(1,3,4-oxadiazol-2-yl)thiophen-3-yl)-2-(naphthalen-1-yl)acetamide (45 mg, 12%). Method [7] m/z 357.9 (M+Na); retention time=5.919. 1H-NMR (CDCl3) δ 8.18 (d, J=1.1 Hz, 1H), 8.16 (d, J=1.4 Hz, 1H), 8.05 (d, J=8.3 Hz, 1H), 7.88 (d, J=8.0 Hz, 2H), 7.61-7.41 (m, 5H), 4.27 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450363B2
Source datasetuspto-grants-2013_05
ORD IDord-fd99f918c5b44bcab991765918e6ec0f
Source noteuspto-grants-2013_05