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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 531177Generated: October 30, 2026

Hydrazine → 2-Hydrazino-5,6-dihydrobenzo[h]quinazoline

https://huagongshe.com/reaction/531177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant2-Chloro-5,6-dihydrobenzo[h]quinazolineHCID 53486027—
SolventPyridineHCID 1049—
Product2-Hydrazino-5,6-dihydrobenzo[h]quinazolineHCID 59774515—

Reaction Steps

Crude 2-chloro-5,6-dihydrobenzo[h]quinazoline was heated at 120° C. in a mixture of anhydrous pyridine (20 mL) and anhydrous hydrazine (7 mL) for 4 h. The solvent was removed under vacuum and the residue was partitioned between chloroform and 1M aqueous potassium carbonate solution. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum to give 2-hydrazinyl-5,6-dihydrobenzo[h]quinazoline as a white solid, 2.16 g. 1H NMR (CDCl3, 300 MHz) 8.27 (d, 1H), 8.20 (s, 1H), 7.35 (m, 2H), 7.21 (d, 1H), 6.42 (s, 1H), 4.00 (br s, 2H), 2.91 (m, 2H), 2.80 (m, 2H) ppm; 13C NMR (CDCl3, 75 MHz) 164.29, 160.00, 156.72, 139.87, 132.83, 131.02, 128.25, 127.25, 125.47, 119.03, 28.54, 24.24; MS (ES) 213 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09353126B2
Source datasetuspto-grants-2016_05
ORD IDord-d6ba9eb7f87a43808d00ba41e8463c4f
Source noteuspto-grants-2016_05