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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274647Generated: November 4, 2026

Dichloromethane → HCID 22119958, compound

https://huagongshe.com/reaction/1274647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 22119820HCID 22119820—
ReactantHCID 178477797HCID 178477797—
CatalystDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22119958HCID 2211995865.7%

Reaction Steps

N,N-Dimethylformamide (8 drops) is added to a mixture of 5-[3,6-dihydro-3-methyl-2,6-dioxo-4-(trifluoromethyl)-1(2H)-pyrimidinyl]-α,α-dimethyl-1,2-benzisothiazole-3-acetic acid (0.800 g, 0.00194 mol) and methylene chloride. The mixture is cooled on an ice bath and oxalyl chloride (2.0 M in methylene chloride, 2.42 ml, 0.00484 mol) is added. The resultant mixture is stirred one hour on an ice bath and concentrated in vacuo. The residue is taken up in tetrahydrofuran. The resultant solution is added dropwise to a mixture of methyl zinc chloride (2.0 M, 0.970 ml, 0.00194 mol) in tetrahydrofuran, followed by addition of palladium tetrakistriphenylphosphine (0.220 g, 0.000190 mol). The resultant mixture is stirred overnight at room temperature, quenched with 10% hydrochloric acid, and extracted with ethyl acetate. The organic layer is washed with saturated sodium bicarbonate and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to an orange solid. The solid is chromatographed on silica gel to afford the title compound as an off-white solid (0.270 g, 65.7%, mp 195-196° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156700
Source datasetuspto-grants-2000_12
ORD IDord-bbe64eb8f57944ca8827d07cdec0fce8
Source noteuspto-grants-2000_12