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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256999Generated: November 1, 2026

4-(2-thienyl)-8-chloro-3-methoxy-2,5-dioxo-2,5-dihydro-1H-benz[b]azepine → HCID 178518635, compound

https://huagongshe.com/reaction/2256999

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(2-thienyl)-8-chloro-3-methoxy-2,5-dioxo-2,5-dihydro-1H-benz[b]azepineHCID 18980043—
SolventHCl tetrahydrofuranHCID 18422008—
ProductHCID 178518635HCID 17851863525.1%

Reaction Steps

A solution of 4-(2-thienyl)-8-chloro-3-methoxy-2,5-dioxo-2,5-dihydro-1H-benz[b]azepine (0.20 g) in 2.4N HCl/THF (1:1, 200 mL) was allowed to stir at room temperature for 1 hour followed by heating to 50° C. for 1 hour. The reaction mixture was partitioned between ether and water. The organic portion was dried (MgSO4), filtered, and concentrated in vacuo. The residue was recrystallized twice from ethyl acetate/hexanes to afford the title compound (0.048 g); mp 231°-233° C. (dec.); NMR: 11.70 (bs, 1), 7.72 (d, 1, J=8.6), 7.62-7.60 (m,2), 7.40 (d, 1, J=1.9), 7.32 (dd, 1, J=8.6, 2.0), 7.10 (m, 1). Analysis for C14H8O3NClS 0.25 H2O.: Calculated: C, 54.29; H, 2.76; N, 4.51; Found C, 54.38; H, 2.90; N, 4.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656626
Source datasetuspto-grants-1997_08
ORD IDord-5ed356c1b0964d10817e58494d1fa2c9
Source noteuspto-grants-1997_08