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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065914Generated: November 3, 2026

Diisopropylethylamine → HCID 136170273, compound

https://huagongshe.com/reaction/2065914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 67027015HCID 67027015—
ReactantHCID 178436626HCID 178436626—
SolventDichloromethaneHCID 6344—
ProductHCID 136170273HCID 13617027328.9%

Reaction Steps

To a solution of 5,6-diethyl-nicotinic acid hydrochloride (920 mg, 4.3 mmol) and Hünig's base (2.76 g, 21 mmol) in DCM (50 mL) is added TBTU (1.785 g, 5.55 mmol) and the mixture is stirred at rt for 5 min. 3-Ethyl-4,N-dihydroxy-5-methyl-benzamidine (1.14 g, 4.7 mmol) is added and the mixture stirred for 0.5 h. The mixture is diluted with DCM, washed with sat. aq. NaHCO3 solution, dried over MgSO4, filtered and concentrated. The crude 5,6-diethyl-nicotinic acid (3-ethyl-4,N-dihydroxy-5-methyl-benzamidine) ester (LC-MS: tR=0.79 min) is dissolved in dioxane (50 mL) and heated to 100° C. for 18 h. The solvent is evaporated and the crude product is purified by FC on silica gel eluting with heptane:EA 10:1 to give 4-[5-(5,6-diethyl-pyridin-3-yl)-[1,2,4]oxadiazol-3-yl]-2-ethyl-6-methyl-phenol (0.42 g) as a solid; LC-MS: tR=1.03 min, [M+1]+=338.09.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288554B2
Source datasetuspto-grants-2012_10
ORD IDord-76625bef59204222b60b49a4028b7406
Source noteuspto-grants-2012_10