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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631826Generated: October 30, 2026

N-BOC-ethylenediamine → Ethyl 2-[2-(tert-butoxycarbonylamino)ethylamino]-5-methylamino-thiazole-4-carboxylate

https://huagongshe.com/reaction/631826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-BOC-ethylenediamineHCID 187201—
Reactant3'-O-ethyl-N,N-diisopropylphosphoramiditeHCID 195451—
ReactantEthyl 2-bromo-5-(methylamino)-1,3-thiazole-4-carboxylateHCID 53613688—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-[2-(tert-butoxycarbonylamino)ethylamino]-5-methylamino-thiazole-4-carboxylateHCID 89825793—

Reaction Conditions

Temperature100 °C

Reaction Steps

Ethyl 2-bromo-5-methylamino-thiazole-4-carboxylate (546 mg, 2.059 mmol) and tert-butyl N-(2-aminoethyl)carbamate (1.3 g, 8.11 mmol) were combined in anhydrous 1,4-dioxane (15 ml). EDIPA (3 ml, 17.2 mmol) was added and the mixture was heated in a sealed tube for 23 hours at 100° C. The mixture was cooled to room temperature and partitioned between DCM and a saturated solution of sodium bicarbonate. Layers were separated, the aqueous phase was extracted twice with DCM and the combined organic layers were dried over sodium sulfate. The solvent was removed under reduced pressure and the residue was purified by column chromatography (silica, gradient of 30 to 100% ethyl acetate in heptane) to yield 185 mg (0.537 mmol, 26%) MS(ESI) m/z=345.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321724B2
Source datasetuspto-grants-2016_04
ORD IDord-6c7966313d6e483986bb44f2c77ff9be
Source noteuspto-grants-2016_04