Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45396Generated: October 28, 2026

Benzylamine → 2-(Tert-butoxycarbonylamino)-4-methylthiazole-5-carboxylic acid benzylamide

https://huagongshe.com/reaction/45396

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantDiisopropylamineHCID 7912—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantN-Boc-amino-4-methylthiazole-5-carboxylic acidHCID 2756770—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-(Tert-butoxycarbonylamino)-4-methylthiazole-5-carboxylic acid benzylamideHCID 8664252150.1%

Reaction Steps

To a stirred solution of 2-(tert-butoxycarbonylamino)-4-methylthiazole-5-carboxylic acid (2.97 g, 11.50 mmol) and diisopropylamine (8.5 mL, 48.70 mmol) in dichloromethane (40 mL) was added N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (2.25 g, 11.50 mmol) and 1-hydroxybenzotriazole (2.02 g, 14.80 mmol). After 30 min benzylamine (1.7 mL, 15.60 mmol) was added. The resultant mixture was stirred at ambient temperature over 8 h, diluted with ethyl acetate, washed with water and brine, dried over anhydrous sodium sulfate, 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 2-(tert-butoxycarbonylamino)-4-methylthiazole-5-carboxylic acid benzylamide (2.00 g, 50% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541457B2
Source datasetuspto-grants-2013_09
ORD IDord-a0ca25b0155045efa99fa0e55e339a4f
Source noteuspto-grants-2013_09