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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1871975Generated: November 2, 2026

N-(tert-butoxycarbonyl)glycine → Ethyl 2-(2-(2-aminoacetamido)thiazol-4-yl)acetate

https://huagongshe.com/reaction/1871975

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(tert-butoxycarbonyl)glycineHCID 78288—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Thiazoleacetic acid, 2-amino-, ethyl esterHCID 104454—
ReactantPyBroPHCID 2733179—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
ProductEthyl 2-(2-(2-aminoacetamido)thiazol-4-yl)acetateHCID 54551034—

Reaction Steps

A mixture of N-(tert-butoxycarbonyl)glycine (3.1 g), 2-amino-4-thiazoleacetic acid ethyl ester (3 g) and bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (7.54 g) in dimethylformamide (20 ml) was treated with N,N-diisopropylethylamine (6 ml). After 25 minutes N,N-dimethyl-4-aminopyridine (1.96 g) was added. After 24 hours the mixture was partitioned between ethyl acetate and brine. The organic phase was washed with saturated aqueous sodium bicarbonate, brine, IN HCl and brine, dried (MgSO4) and evaporated. The residue was purified by chromatography eluting with 50% ethyl acetate in isohexane. The product (0.77 g) was dissolved in dichloromethane (25 ml) and trifluoroacetic acid (10 ml). After 2 hours the mixture was evaporated. The residue was partitioned between ethyl acetate and sodium bicarbonate solution. The aqueous phase was repeatedly extracted with ethyl acetate. The combined extracts were dried (MgSO4) and evaporated. Yield 0.41 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107297
Source datasetuspto-grants-2000_08
ORD IDord-5dbda3ddb30a486ba67918a915667c9a
Source noteuspto-grants-2000_08