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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45315Generated: October 29, 2026

Benzylamine → 2-Amino-4-benzylthiazole-5-carboxylic Acid Benzylamide

https://huagongshe.com/reaction/45315

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Amino-4-benzylthiazole-5-carboxylic acidHCID 82225511—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-Amino-4-benzylthiazole-5-carboxylic Acid BenzylamideHCID 8664251365%

Reaction Steps

To a solution of 2-amino-4-benzylthiazole-5-carboxylic acid (0.033 g, 0.14 mmol) and diisopropylethylamine (0.08 mL, 0.46 mmol) in N,N-dimethylformamide (5 mL) was added N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.039 g, 0.20 mmol), followed by the addition of 1-hydroxybenzotriazole (0.026 g, 0.19 mmol). After 30 minutes, benzylamine (0.02 mL, 0.18 mmol) was added. The reaction mixture was stirred at ambient temperature for 12 h, diluted with ethyl acetate, washed with water, brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash column chromatography eluting with ethyl acetate/hexanes (5/95 to 100/0) to afford the title compound (0.029 g, 65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541457B2
Source datasetuspto-grants-2013_09
ORD IDord-3f803fe591544eb0ae89adf6407e75c4
Source noteuspto-grants-2013_09