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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274648Generated: November 4, 2026

2-Dimethylaminopyridine → HCID 22119992, compound

https://huagongshe.com/reaction/1274648

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-DimethylaminopyridineHCID 21885—
ReactantOxalyl chlorideHCID 65578—
ReactantMethanesulfonamideHCID 72879—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 22119820HCID 22119820—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
ProductHCID 22119992HCID 2211999213.5%

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 (2.00 g, 0.00484 mol) and methylene chloride. The mixture is cooled on an ice bath and oxalyl chloride (2.0 M in methylene chloride, 6.05 ml, 0.0121 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. Methylsulfonamide (0.690 g, 0.00726 mol) is added, followed by ethyldiisopropylamine (0.940 g, 0.00727 mol) and dimethylaminopyridine (0.100 g). The resultant mixture is stirred at room temperature and filtered. The filtrate is concentrated in vacuo and the residue is filtered through silica gel with hexanes:ethyl acetate. The filtrate is concentrated in vacuo to a tan solid. The solid is suspended in methylene chloride, stirred, and refiltered to give the title compound as a white solid (0.320 g, 13.5%, mp 264-265° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06156700
Source datasetuspto-grants-2000_12
ORD IDord-8fab8baf12804d5089e953babd489946
Source noteuspto-grants-2000_12