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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733960Generated: November 1, 2026

(2-Chloro-4-nitrophenyl)(6,7,8,9-tetrahydro-5H-pyrido[3,2-b]azepin-5-yl)methanone → HCID 19438743, compound

https://huagongshe.com/reaction/1733960

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Chloro-4-nitrophenyl)(6,7,8,9-tetrahydro-5H-pyrido[3,2-b]azepin-5-yl)methanoneHCID 19699064—
ReactantChloride dihydrateHCID 21226388—
SolventMethanolHCID 887—
ProductHCID 19438743HCID 1943874385.7%

Reaction Steps

A mixture of 3.31 g of 6,7,8,9-tetrahydro-5-(2-chloro-4-nitrobenzoyl)-5H-pyrido[3,2-b]azepine and 6.78 g of stannus chloride dihydrate (SnCl2.2H2O) in 200 ml of methanol is refluxed for 2 hours under argon. The solvent is removed under vacuum and 5 ml of saturated NaHCO3 solution and solid NaHCO3 added to bring the pH to 7. The mixture is extracted with ethyl acetate, the extract filtered through diatomaceous earth and the filtrate washed with saturated NaHCO3, H2O, brine and dried (Na2SO4). The filtrate is passed through a thin pad of hydrous magnesium silicate and the filtrate concentrated to dryness to give 2.58 g of an amorphous solid. Anal. Calc'd for C16H16ClN3O; C,59.9; H,5.7; N,13.1; C1, 11.1 Found: C,60.5; H,5.0; N,12.9; Cl,11.6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05532235
Source datasetuspto-grants-1996_07
ORD IDord-1cf4529766dd4497becb9e5e29b67966
Source noteuspto-grants-1996_07