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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2063204Generated: November 4, 2026

Triethylamine → HCID 67239447, compound

https://huagongshe.com/reaction/2063204

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPropylphosphonic anhydrideHCID 111923—
ReactantFurazanamine, 4-(acetylamino)-HCID 536687—
Reactant2-Chloro-4-(methylsulfonyl)benzoic acidHCID 735863—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 67239447HCID 67239447—

Reaction Steps

173 mg (0.5 mmol) of 2-chloro-4-(methylsulfonyl)benzoic acid and 191 mg (0.505 mmol) of N-(4-amino-1,2,5-oxadiazol-3-yl)acetamide are dissolved in 5 ml of dichloroethane at RT and treated with 0.071 ml (0.5 mmol) of triethylamine, 31 mg (0.25 mmol) of DMAP and 483 mg (0.76 mmol) of 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane 2,4,6-trioxide (50% solution in THF). The reaction mixture is stirred for 24 h at RT and subsequently filtered through a glass frit. The residue is washed twice using in each case 1 ml of CH2Cl2. The filtrate is passed over a silica-gel-filled SPE cartridge and eluted twice using in each case 5 ml of a mixture of ethyl acetate/methyl tert-butyl ester (1:1). The organic phase is dried over Na2SO4 and evaporated. The residue is purified by preparative HPLC using acetonitrile/water. Yield 16 mg (9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288316B2
Source datasetuspto-grants-2012_10
ORD IDord-5f93d84652ca4fbf8628a74b4b6561a3
Source noteuspto-grants-2012_10