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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2259525Generated: November 1, 2026

Triethylamine → 5-(((Methanesulfonyl)oxy)methyl)-2-methylthiazolo[5,4-b]pyridine

https://huagongshe.com/reaction/2259525

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant2-methylThiazolo[5,4-b]pyridine-5-methanolHCID 19002884—
SolventDichloromethaneHCID 6344—
Product5-(((Methanesulfonyl)oxy)methyl)-2-methylthiazolo[5,4-b]pyridineHCID 22068764—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of the alcohol of Step 6 (303 mg, 1.68 mmol) in 17 mL of CH2Cl2 at -40° C., triethylamine (350 μl, 2.5 mmol) and methane-sulfonyl chloride (170 μl, 2.2 mmol) were added and the solution was stirred at -40° C. for 30 min and at 0° C. for 2 hr. Saturated aq. NaHCO3 was added and the product was extracted in CH2C12, dried over Na2SO4, concentrated, and the remaining water was stripped with toluene twice.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05472964
Source datasetuspto-grants-1995_12
ORD IDord-61836e9bf8f24e73a97f3cc854334b1f
Source noteuspto-grants-1995_12