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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2228494Generated: October 30, 2026

Sodium hydride → HCID 18470640, compound

https://huagongshe.com/reaction/2228494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantBromocyclobutaneHCID 78110—
ReactantHCID 18470651HCID 18470651—
SolventDimethylformamideHCID 6228—
ProductHCID 18470640HCID 1847064035.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

4-Amino-6-hydroxy-7-methoxy-2-[4-(4-morpholinecarbonyl)-1,4-diazepan-1-yl]quinoline (200 mg, 0.0005 mol) and cyclobutyl bromide (75 mg, 0.00055 mol) were added to a suspension of sodium hydride (20 mg, 0.0005 mol) in dimethylformamide (5 ml), and the reaction stirred under a nitrogen atmosphere at 50° C. for 18 hours. On cooling, the mixture was partitioned between ethyl acetate (15 ml) and water (15 ml), and the aqueous layer further extracted with ethyl acetate (30 ml). The combined organic extracts were dried (MgSO4), filtered and evaporated under reduced pressure. The crude product was purified on silica gel eluting with a solvent gradient of 0.880 aqueous ammonia: methanol:dichloromethane (0:0:100 to 1:10:90 v/v) to give the title compound as a foam (80 mg, 35%). Rf 0.65 (0.880 aqueous ammonia:methanol:dichloromethane 2:14:84, v/v). MS m/z 456 (MH)+. Found: C, 56.54; H, 6.60; N, 13.83; C24H33N5O4 0.6 CH2Cl2 0.8 H2O, requires C, 56.72; H, 6.93; N, 13.44%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06417194B1
Source datasetuspto-grants-2002_07
ORD IDord-869fd1e7a3944c5a8affe1ccb76b5752
Source noteuspto-grants-2002_07