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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429751Generated: October 28, 2026

Triethylamine → N-(tert-butyloxycarbonyl)-3-(4-thiazolyl)-L-alanyl-L-proline benzyl ester

https://huagongshe.com/reaction/429751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantProline benzyl ester hydrochlorideHCID 2733413—
Reactant(S)-2-((tert-Butoxycarbonyl)amino)-3-(thiazol-4-yl)propanoic acidHCID 2734486—
SolventTetrahydrofuranHCID 8028—
ProductN-(tert-butyloxycarbonyl)-3-(4-thiazolyl)-L-alanyl-L-proline benzyl esterHCID 5375321590.5%

Reaction Steps

A solution of N-(tert-butyloxycarbonyl)-3-(4-thiazolyl)-L-alanine (2.72 g, 10 mmol), L-proline benzyl ester hydrochloric acid (2.42 g, 10 mmol), and HOBT (135 mg, 1 mmol) in tetrahydrofuran (60 ml) was added triethylamine (1.4 ml, 10 mmol) and DCC (2.43 g, 11.8 mmol) and the resulting mixture was stirred for 18 h at room temperature. After the precipitation which appeared was filtered off, the filtrate was concentrated in vacuo. The residue (5.5 g) was subjected to silica gel column chromatography with Lobar® column C (Merck inc.) (toluene:acetone=9:1) to give 4.16 g of the compound (30).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06319902B1
Source datasetuspto-grants-2001_11
ORD IDord-c5a2b102ceb94cbcb41b2e153432e64e
Source noteuspto-grants-2001_11