Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178261Generated: October 29, 2026

4-Nitrophenyl benzo[d]thiazol-2-ylcarbamate → 6-(1-(Benzo[d]thiazol-2-ylcarbamoyl)-1,2,3,4-tetrahydroquinolin-7-yl)-3-phenylpicolinic acid

https://huagongshe.com/reaction/2178261

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl benzo[d]thiazol-2-ylcarbamateHCID 59418676—
ReactantMethyl 3-phenyl-6-(1,2,3,4-tetrahydroquinolin-7-yl)picolinateHCID 59418700—
SolventAcetonitrileHCID 6342—
Product6-(1-(Benzo[d]thiazol-2-ylcarbamoyl)-1,2,3,4-tetrahydroquinolin-7-yl)-3-phenylpicolinic acidHCID 46841062—
ProductMethyl 6-(1-(benzo[d]thiazol-2-ylcarbamoyl)-1,2,3,4-tetrahydroquinolin-7-yl)-3-phenylpicolinateHCID 59418756—

Reaction Steps

A mixture of methyl 3-phenyl-6-(1,2,3,4-tetrahydroquinolin-7-yl)picolinate (29H) (17 mg, 0.049 mmol) and 4-nitrophenyl benzo[d]thiazol-2-ylcarbamate (19) (15.5 mg, 0.049 mmol) in anhydrous CH3CN (0.8 mL) was heated to reflux for 6 hours, cooled to rt, concentrated under reduced pressure, and the crude material was purified by column chromatography on silica gel eluting with a gradient of PE:EtOAc 72:28-55:45, to provide the desired product methyl 6-(1-(benzo[d]thiazol-2-ylcarbamoyl)-1,2,3,4-tetrahydroquinolin-7-yl)-3-phenylpicolinate (29I): 1H NMR (300 MHz, CDCl3) δ 8.23 (1H, d), 8.13 (1H, d), 7.85-7.76 (3H, m), 7.66 (1H, d), 7.48-7.35 (4H, m), 7.34-7.28 (2H, m), 6.89 (1H, d), 3.98 (2H, t), 3.71 (3H, s), 2.85 (2H, t), 2.09 (2H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067928B2
Source datasetuspto-grants-2015_06
ORD IDord-5e2eb5afd2c449288b4b16d856e91991
Source noteuspto-grants-2015_06