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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2098062Generated: October 31, 2026

HCID 68754558, compound → HCID 178520285, compound

https://huagongshe.com/reaction/2098062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68754558HCID 68754558—
ReactantHCID 68758750HCID 68758750—
ReactantHCID 178509325HCID 178509325—
ProductHCID 178520285HCID 178520285—
ProductHCID 178520286HCID 178520286—

Reaction Steps

2-(5-(trifluoromethyl)quinolin-7-yl)acetic acid and the mixture of 2-(7-(trifluoromethyl)quinolin-5-yl)acetic acid (28.3 mg, 0.11 mmol) and 4-bromo-3-(4H-1,2,4-triazol-3-yl)thiophen-2-amine (23 mg, 0.094 mmol) were treated according to protocol A. The crude product mixture was purified by HPLC to afford N-(4-bromo-3-(4H-1,2,4-triazol-3-yl)thiophen-2-yl)-2-(5-(trifluoromethyl)quinolin-7-yl)acetamide and N-(4-bromo-3-(4H-1,2,4-triazol-3-yl)thiophen-2-yl)-2-(7-(trifluoromethyl)quinolin-5-yl)acetamide. LCMS method [13], retention time (min) 10.100 and 10.386; MS (ESI) 482.0 (MH+, 79Br); 1H NMR (300 MHz, CD3OD) δ 9.01 (dd, J=4.3, 1.6 Hz, 1H), 8.62 (d, J=8.4 Hz, 1H), 8.41 (s, 1H), 7.98 (s, 1H), 7.70 (dd, J=8.7, 4.3 Hz, 1H), 4.50 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450363B2
Source datasetuspto-grants-2013_05
ORD IDord-4f4c9b5382984c119e8e735ddbea11a8
Source noteuspto-grants-2013_05