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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2178240Generated: October 29, 2026

4-Nitrophenyl benzo[d]thiazol-2-ylcarbamate → Tert-butyl 6-(4-(benzo[d]thiazol-2-ylcarbamoyl)-1-methyl-1,2,3,4-tetrahydroquinoxalin-6-yl)picolinate

https://huagongshe.com/reaction/2178240

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrophenyl benzo[d]thiazol-2-ylcarbamateHCID 59418676—
ReactantTert-butyl 6-(1-methyl-1,2,3,4-tetrahydroquinoxalin-6-yl)picolinateHCID 59418755—
SolventAcetonitrileHCID 6342—
ProductTert-butyl 6-(4-(benzo[d]thiazol-2-ylcarbamoyl)-1-methyl-1,2,3,4-tetrahydroquinoxalin-6-yl)picolinateHCID 5941866785.2%

Reaction Steps

A mixture of tert-butyl 6-(1-methyl-1,2,3,4-tetrahydroquinoxalin-6-yl)picolinate (25G) (36 mg, 0.11 mmol) and 4-nitrophenyl benzo[d]thiazol-2-ylcarbamate (19) (42 mg, 0.13 mmol) in anhydrous acetonitrile (1.0 mL) was heated to reflux for 3 hours, cooled to rt, concentrated under reduced pressure, and the crude material was purified by flash column chromatography on silica gel eluting with a gradient of PE:EtOAc 100:0-70:30, to provide 47 mg (85%) of the desired product tert-butyl 6-(4-(benzo[d]thiazol-2-ylcarbamoyl)-1-methyl-1,2,3,4-tetrahydroquinoxalin-6-yl)picolinate (25H): 1H NMR (300 MHz, CDCl3) δ 8.14 (1H, s), 7.88-7.77 (2H, m), 7.74 (2H, d), 7.54 (1H, d), 7.34 (1H, t), 7.22 (1H, t), 6.71 (1H, d), 3.97 (2H, t), 3.49 (2H, t), 3.02 (3H, s), 1.56 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067928B2
Source datasetuspto-grants-2015_06
ORD IDord-4ec840ae22f14c938aacd72503c4a0f0
Source noteuspto-grants-2015_06