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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856961Generated: October 30, 2026

(3-Amino-6-iodo-1-benzofuran-2-yl)(2,4-dichlorophenyl)methanone → (3-Amino-8-benzyl-5,6,7,8-tetrahydro-furo[3,2-g]quinolin-2-yl)-(2,4-dichloro-phenyl)methanone

https://huagongshe.com/reaction/856961

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Amino-6-iodo-1-benzofuran-2-yl)(2,4-dichlorophenyl)methanoneHCID 21864959—
Reactant1-Benzyl-7-hydroxy-1,2,3,4-tetrahydro-quinoline-6-carbonitrileHCID 21864969—
Product(3-Amino-8-benzyl-5,6,7,8-tetrahydro-furo[3,2-g]quinolin-2-yl)-(2,4-dichloro-phenyl)methanoneHCID 2186495429%

Reaction Steps

This compound was prepared from 1-benzyl-7-hydroxy-1,2,3,4-tetrahydro-quinoline-6-carbonitrile (20 mg, 0.08 mmol) from step 4 in the manner described for [(3-amino-6-iodo-benzofuran-2-yl)-(2,4-dichloro-phenyl)-methanone, affording 10 mg (29%) of the title compound as a yellow solid. 1H-NMR (CDCl3) δ 7.44–7.40 (m, 2H), 7.33–7.22 (m, 4H), 7.18 (s, 1H), 7.15–7.13 (m, 2H), 6.25 (s, 1H), 5.96 (bs, 2H), 4.52 (s, 2H), 3.47 (t, J=6.0 Hz, 2H), 2.89 (t, J=5.9 Hz, 2H), 2.03 (m, 2H); MS LC-MS (MH+=451.3), LC MS RT: 3.81 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07144885B2
Source datasetuspto-grants-2006_12
ORD IDord-616dfb6bee5f4bb09e4f831d528ac9ef
Source noteuspto-grants-2006_12