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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 579370Generated: October 31, 2026

(2-Oxo-1,2-dihydroquinolin-3-yl)boronic acid → HCID 136341349, compound

https://huagongshe.com/reaction/579370

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Oxo-1,2-dihydroquinolin-3-yl)boronic acidHCID 49757966—
Reactant5-Bromo-N-methyl-N-(2,2,6,6-tetramethylpiperidin-4-yl)-1,3,4-thiadiazol-2-amineHCID 86727129—
ProductHCID 136341349HCID 136341349—

Reaction Steps

Following a similar procedure as described for Step 3 in Example 101, (2-oxo-1,2-dihydroquinolin-3-yl)boronic acid and 5-bromo-N-methyl-N-(2,2,6,6-tetramethylpiperidin-4-yl)-1,3,4-thiadiazol-2-amine (858 mg, 2.57 mmol) were reacted to provide the crude product, which was purified by preparative HPLC under basic condition to give 3-(5-(methyl(2,2,6,6-tetramethylpiperidin-4-yl)amino)-1,3,4-thiadiazol-2-yl)quinolin-2(1H)-one (14 mg, MS: 398.2 [M+H+], LCMS Rt=0.51 min (LCMS method D); 1H NMR (400 MHz, METHANOL-d4) δ ppm 8.74 (s, 1H), 7.67-7.80 (m, 1H), 7.47-7.57 (m, 1H), 7.31 (d, J=8.08 Hz, 1H), 7.19-7.27 (m, 1H), 4.34 (br. s., 1H), 2.99 (s, 3H), 1.71 (dd, J=12.63, 3.03 Hz, 2H), 1.50 (t, J=12.38 Hz, 2H), 1.28 (s, 6H), 1.10-1.23 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040712B2
Source datasetuspto-grants-2015_05
ORD IDord-9cb155e9a99349cc8c2c6ed3f2bfdf74
Source noteuspto-grants-2015_05