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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2040100Generated: October 30, 2026

4(5H)-Thiazolone, 2-amino- → 4-[2-Fluoro-4-[(2-imino-4-oxo-1,3-thiazolidin-5-ylidene)methyl]phenoxy]naphthalene-1-carbonitrile

https://huagongshe.com/reaction/2040100

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4(5H)-Thiazolone, 2-amino-HCID 11175—
Reactant4-(2-Fluoro-4-formyl-phenoxy)-naphthalene-1-carbonitrileHCID 86623141—
Product4-[2-Fluoro-4-[(2-imino-4-oxo-1,3-thiazolidin-5-ylidene)methyl]phenoxy]naphthalene-1-carbonitrileHCID 140529023—

Reaction Steps

4-[2-Fluoro-4-(2-imino-4-oxo-thiazolidin-5-ylidenemethyl)-phenoxy]-naphthalene-1-carbonitrile was prepared using 2-amino-thiazol-4-one and 4-(2-Fluoro-4-formyl-phenoxy)-naphthalene-1-carbonitrile following General Procedure C. 1H NMR (400 MHz, DMSO-d6) δ 9.54 (br, 1H), 9.25 (br, 1H), 8.42 (d, J=8.21 Hz, 1H), 8.15 (d, J=8.21 Hz, 1H), 8.08 (d, J=7.82 Hz, 1H), 7.91 (m, 1H), 7.81 (m, 1H), 7.7 (dd, J=12.13 and 2.34 Hz, 1H), 7.64 (s, 1H), 7.49-7.57 (2H), 6.93 (d, J=7.83 Hz, 1H). LC/MS (m/z) [M+1]+390.2 (calculated for C21H13FN3O2S 390.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580832B2
Source datasetuspto-grants-2013_11
ORD IDord-5e7b6bd506cb4c87a1da682dbf2c631d
Source noteuspto-grants-2013_11