Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085830Generated: October 27, 2026

N-BOC-ethylenediamine → t-Butyl [2-(2-amino-5-phenyl-4-thiazolecarboxamido)ethyl]carbamate

https://huagongshe.com/reaction/1085830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BOC-ethylenediamineHCID 187201—
ReactantMethyl 2-amino-5-phenyl-1,3-thiazole-4-carboxylateHCID 664327—
SolventMethanolHCID 887—
Productt-Butyl [2-(2-amino-5-phenyl-4-thiazolecarboxamido)ethyl]carbamateHCID 5405289145.1%

Reaction Steps

5.0 g (21.3 mmol) of methyl 2-amino-5-phenyl-4-thiazolecarboxylate (which was prepared as described in J. Chem. Soc. Perk. Trans. I (1982) 159-164) and 6.84 g (42.7 mmol) of t-butyl (2-aminoethyl)carbamate were heated under reduced pressure for 2 hours at a bath temperature of 140°, whereby the methanol formed was distilled off continuously. After cooling the residue was dissolved in 50 ml of methylene chloride and chromatographed on 200 g of silica gel with a 9:1 mixture of methylene chloride and methanol as the eluting agent. The fractions which were pure according to the thin-layer chromatogram were combined and evaporated under reduced pressure, whereby there were obtained 4.5 g of a red, crystallizing oil. Crystallization from methanol and an ether/hexane mixture yielded 3.48 g (45%) of t-butyl [2-(2-amino-5-phenyl-4thiazolecarboxamido)ethyl]carbamate as beige crystals which were used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011849
Source datasetuspto-grants-1991_04
ORD IDord-3ff7e91cdcca4fb68e4c2864663acb2c
Source noteuspto-grants-1991_04