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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390516Generated: October 30, 2026

Diisopropylethylamine → (5-(3-(3-tert-butyl-1,2,4-thiadiazol-5-ylamino)pyridin-2-yloxy)-3,4-dihydroquinolin-1(2H)-yl)(phenyl)methanone

https://huagongshe.com/reaction/2390516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantPivalamidine hydrochlorideHCID 431752—
Reactant1,1'-Thiocarbonyldi-2(1H)-pyridoneHCID 853162—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant(5-(3-aminopyridin-2-yloxy)-3,4-dihydroquinolin-1(2H)-yl)(phenyl)methanoneHCID 59128866—
SolventDichloromethaneHCID 6344—
Product(5-(3-(3-tert-butyl-1,2,4-thiadiazol-5-ylamino)pyridin-2-yloxy)-3,4-dihydroquinolin-1(2H)-yl)(phenyl)methanoneHCID 5912897614.2%

Reaction Steps

A mixture of (5-(3-aminopyridin-2-yloxy)-3,4-dihydroquinolin-1(2H)-yl)(phenyl)methanone (Example A171d) (224 mg, 0.58 mmol), 1,1′-thiocarbonyldi-2(1H)-pyridone (269 mg, 1.16 mmol) in DCM (10 mL) was agitated at rt for 4 h. The mixture was evaporated and diluted in THF (5 mL), pivalamidine (79 mg, 0.58 mmol) and DIPEA (205 μL, 1.16 mmol) were added and mixture was heated at 80° C. in a sealed tube for 24 h. The solution was cooled down and DEAD (183 μL, 1.16 mmol) was added, mixture was stirred for 2 h. The reaction mixture was evaporated in vacuo and purified using preparative HPLC to afford the final product (40 mg). (M+H)+=486.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273772B2
Source datasetuspto-grants-2012_09
ORD IDord-a73b9dfcd1a2460186c5b607dbe503e7
Source noteuspto-grants-2012_09