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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1482860Generated: October 31, 2026

4-(1,2,3,4-Tetrahydroquinoline-1-sulfonyl)benzoic acid → HCID 86662356, compound

https://huagongshe.com/reaction/1482860

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(1,2,3,4-Tetrahydroquinoline-1-sulfonyl)benzoic acidHCID 2318939—
ReactantHCID 22693688HCID 22693688—
ProductHCID 86662356HCID 86662356—

Reaction Steps

4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)benzoic acid (1) (200 mg, 0.63 mmol) was treated with 6-(2-aminothiazol-4-yl)benzo[d]oxazol-2(3H)-one (198 mg, 0.55 mmol) using method C. The residue was purified using flash chromatography eluting with 0-70% EtOAc in hexanes. The resulting solid was triturated with dichloromethane/hexanes to give 4-(3,4-dihydroquinolin-1(2H)-ylsulfonyl)-N-(4-(2-oxo-2,3-dihydrobenzo[d]oxazol-6-yl)thiazol-2-yl)benzamide as a yellow solid. Yield: 73 mg (22%). 1H-NMR: 8.21 (d, J=8.5 Hz, 2H), 7.84-7.74 (m, 4H), 7.69 (s, 1H), 7.62 (d, J=8.5 Hz, 1H), 7.24-7.19 (m, 1H), 7.15 (d, J=8.5 Hz, 1H), 7.13-7.07 (m, 2H), 3.85-3.78 (m, 2H), 2.45 (t, J=7.0 Hz, 2H), 1.67-1.58 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09416101B2
Source datasetuspto-grants-2016_08
ORD IDord-c07c00b7807b44d19814d7776f5a96b3
Source noteuspto-grants-2016_08