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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670681Generated: October 26, 2026

Stannous Chloride → HCID 44140427, compound

https://huagongshe.com/reaction/1670681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous ChlorideHCID 24479—
Reactant6-Nitro-2-(1,3-benzodioxole-5-yl)-quinazolineHCID 57863156—
SolventEthanolHCID 702—
ProductHCID 44140427HCID 4414042764%

Reaction Steps

A suspension of 6-nitro-2-(1,3-benzodioxol-5-yl)-quinazoline (37 g, 0.126 mol) and SnCl2 2H2O (117.2 g, 0.504 mol) in ethanol (500 ml) was heated at reflux for 1 h. After cooling to r. t., the solvent was removed i.v., chloroform was added and the mixture was basified with ammonia. The precipitate was filtered off and washed with chloroform. The filtrates were collected, washed with water and dried over Na2SO4. The solution was concentrated i.v., and the residue triturated with diisopropyl ether/petroleum ether. The solid was filtered and dried i.v. to give the titled product (21.2 g, 64% yield). C15H11N3O2, MW: 265.27. mp 191-192° C.; 1H NMR (DMSO-d6) 9.24 (s, 1H), 8.05 (dd, 1H), 7.91 (d, 1H), 7.73 (d, 1H), 7.39 (dd, 1H), 7.03 (d, 1H), 6.90 (d, 1H), 6.11 (s, 2H), 5.93 (s, 2H); IR (KBr) 3319, 3203, 1631, 1500, 1446; TLC (CHCl3/MeOH 9/1) Rf=0.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994181B2
Source datasetuspto-grants-2011_08
ORD IDord-e4cd81fd52d64552ac31b8465d76d886
Source noteuspto-grants-2011_08