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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631130Generated: October 30, 2026

Triethylamine → HCID 86638017, compound

https://huagongshe.com/reaction/631130

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 66605829HCID 66605829—
SolventEthyl AcetateHCID 8857—
ProductHCID 86638017HCID 8663801799%

Reaction Steps

To a solution of 3-{4-[(2-hydroxyethyl)amino]-1,2,5-oxadiazol-3-yl}-4-[3-(trifluoromethyl)phenyl]-1,2,4-oxadiazol-5(4H)-one (1.0 g, 2.9 mmol) in ethyl acetate (8.5 mL) was added methanesulfonyl chloride (0.29 mL, 3.7 mmol) in one portion. The reaction was stirred for 5 minutes and triethylamine (0.52 mL, 3.7 mmol) was added, also in one portion. After stirring for an additional 10 minutes, the reaction was quenched with the addition of water (5 mL). The product was extracted with ethyl acetate (2×5 mL), dried over sodium sulfate and concentrated in vacuo to give the desired product (1.2 g, 99%). LCMS calculated for C14H13F3N5O6S (M+H)+: m/z=436.0. 1H NMR (400 MHz, DMSO-d6): δ 8.10 (s, 1H), 7.92 (m, 2H), 7.80 (t, J=8.2 Hz, 1H), 6.77 (t, J=5.9 Hz, 1H), 4.36 (t, J=5.5 Hz, 2H), 3.58 (m, 2H), 3.17 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09320732B2
Source datasetuspto-grants-2016_04
ORD IDord-f9b92e159ad64b268173fbf7328609aa
Source noteuspto-grants-2016_04