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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221343Generated: October 27, 2026

Water → Methanesulfonic acid 3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl ester

https://huagongshe.com/reaction/221343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant[3-(4-Pyridinyl)-1,2,4-oxadiazol-5-yl]methanolHCID 37134678—
SolventDichloromethaneHCID 6344—
ProductMethanesulfonic acid 3-pyridin-4-yl-[1,2,4]oxadiazol-5-ylmethyl esterHCID 57954388—

Reaction Steps

Methanesulfonyl chloride (0.50 ml, 6.50 mmol) was added to a stirred solution of (3-pyridin-4-yl-[1,2,4]oxadiazol-5-yl)methanol (1 g, 5.65 mmol) and triethylamine (0.953 ml, 6.78 mmol) in CH2Cl2 (30 ml) at 0° C. After 10 min, water (20 ml) was added and the aqueous phase extracted with CH2Cl2 (20 ml). The combined organic phases were dried (MgSO4) and evaporated to afford the title compound: RT=2.32 min; m/z (ES+)=256.0 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207147B2
Source datasetuspto-grants-2012_06
ORD IDord-d3ce24e9c3d44bf7bc856bcc84bcd56f
Source noteuspto-grants-2012_06