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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1024452Generated: October 26, 2026

Pyridine → Methyl 2-(4-(4-(4-tert-butylbenzamido)phenyl)thiazole-2-carboxamido)-3-methylbutanoate

https://huagongshe.com/reaction/1024452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-tert-Butylbenzoyl chlorideHCID 74372—
ReactantMethyl 3-methyl-2-(4-(4-nitrophenyl)thiazole-2-carboxamido)butanoateHCID 67150325—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(4-(4-(4-tert-butylbenzamido)phenyl)thiazole-2-carboxamido)-3-methylbutanoateHCID 52935052—

Reaction Steps

Pyridine (0.22 ml) was added to methyl-2-(4-(4-aminophenyl)thiazole-2-carboxamido)-3-methylbutanoate (Intermediate 3, 300 mg) in DCM (4 ml) and the reaction mixture was stirred for 5 minutes. 4-tert-butyl benzoyl chloride (230 mg) was added and reaction mixture was stirred for 16 hours at RT. Organic solvent was concentrated to obtain a sticky solid, which was purified by column chromatography (silica gel, EtOAc-petroleum ether) to obtain title compound as solid. Yield: 235 mg (53%). 1H NMR (DMSO-d6, 300 MHz): δ 10.31 (s, 1H), 8.83 (d, 1H), 8.36 (s, 1H), 8.10 (d, 2H), 7.91 (dd, 4H), 7.56 (d, 2H), 4.38 (t, 1H), 3.68 (s, 3H), 2.35 (m, 1H), 1.31 (s, 9H), 0.98 (t, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722901B2
Source datasetuspto-grants-2014_05
ORD IDord-91265a575b4a4a66b9c36e0a94741861
Source noteuspto-grants-2014_05