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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397899Generated: October 25, 2026

2-Amino-4-phenylthiazole → 4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)-N-(4-phenylthiazol-2-yl)benzamide

https://huagongshe.com/reaction/1397899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-4-phenylthiazoleHCID 40302—
Reactant4-(1,2,3,4-Tetrahydroquinoline-1-sulfonyl)benzoic acidHCID 2318939—
Product4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)-N-(4-phenylthiazol-2-yl)benzamideHCID 16547676—

Reaction Steps

4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzoic acid (1) (100 mg, 0.32 mmol) was treated with 4-phenylthiazol-2-amine (43 mg, 0.24 mmol) using method B. The residue was purified using flash chromatography eluting with 0-40% EtOAc in hexanes to give 4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)-N-(4-phenylthiazol-2-yl)benzamide as a white solid. Yield: 43 mg, (37%). 1H-NMR: 8.21 (d, J=8.5 Hz, 2H), 7.95 (d, J=8.0 Hz, 2H), 7.78-7.73 (m, 3H), 7.62 (d, J=8.5 Hz, 1H), 7.47-7.42 (t, J=7.5 Hz, 2H), 7.36-7.32 (m, 1H), 7.24-7.08 (m, 3H), 3.84-3.80 (m, 2H), 2.45 (t, J=7.0 Hz, 2H), 1.66-1.59 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901306B2
Source datasetuspto-grants-2014_12
ORD IDord-2c537a72d4d04e2b823fc490df8ffe2a
Source noteuspto-grants-2014_12