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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1938804Generated: October 31, 2026

Acetone → 2-Methyl-[(4-nitro-5-tetrazolo[1,5-a]quinolinyl)amino]-2-propanol

https://huagongshe.com/reaction/1938804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantDimethylformamideHCID 6228—
ReactantSodium AzideHCID 33557—
Reactant1-((2-Chloro-3-nitroquinolin-4-yl)amino)-2-methylpropan-2-olHCID 12051696—
SolventWaterHCID 962—
Product2-Methyl-[(4-nitro-5-tetrazolo[1,5-a]quinolinyl)amino]-2-propanolHCID 15489758—

Reaction Steps

Sodium azide (19.5 g, 0.3 moles), 2-methyl-[(2-chloro-3-nitroquinoline-4-yl)amino]-2-propanol (29.6 g, 0.10 mole, U.S. Pat. No. 4,988,815 Example 12) and N,N-dimethylformamide (100 mL) were added to a jacketed 1 liter round bottom flask with the outside portion containing acetone. The reaction mixture was stirred with a stirring bar and the acetone refluxed to provide a constant internal reaction temperature of 53° C. After 18 hours the reaction mixture was diluted with water (100 mL). The resulting yellow precipitate was isolated by filtration then washed with 50% N,N-dimethylformamide/water until the washes became light colored. The yellow/green solid was then washed with water, pressed dry and washed with ether. The solid was air dried to provide 27.2 g of crude product as a yellow/light green solid. This material was recrystallized form ethanol/dichloromethane to provide 2-methyl-[(4-nitro-5-tetrazolo[1,5-a]quinolinyl)amino]-2-propanol as a yellow crystalline solid, m.p. 204° C. (dec.). Analysis: Calculated for: C13H14N6O3 : % C, 51.65; % H, 4.67; % N, 27.8; Found: % C, 51.30; % H, 4.69; % N, 27.43.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05693811
Source datasetuspto-grants-1997_12
ORD IDord-cd7ef4ed109c4ae5a5308ca21ed46c59
Source noteuspto-grants-1997_12