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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419925Generated: October 30, 2026

Thionyl Chloride → HCID 59679997, compound

https://huagongshe.com/reaction/419925

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant3-Hydroxymethyl-6-(2-nitrophenyl)imidazo[2,1-b]thiazoleHCID 25232523—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 59679997HCID 59679997—

Reaction Steps

To a stirred solution of [6-(2-Nitro-phenyl)-imidazo[2,1-b]thiazol-3-yl]-methanol (1.0 g, 3.63 mmol) in anhydrous dichloromethane (15 ml) was slowly added thionyl chloride (2 ml, 7.5 eq). The solution turned homogenous, followed by development of a yellow precipitate. After 5 minutes, a catalytic amount of DMF (1 drop) was added and the mixture was stirred for 1 hour, concentrated to dryness, chased with CH2Cl2 (2×) then Ether (1×), and dried under reduced pressure. 1.53 g of yellow solid was obtained, and assumed to be quantitative yield. (MS, M++H=294.0)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093401B2
Source datasetuspto-grants-2012_01
ORD IDord-42d9668393b745e498ca1021eccc9edc
Source noteuspto-grants-2012_01