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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 218308Generated: October 26, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → (s)-Tert-butyl 4-(tert-butoxycarbonylamino)-5-(2-carbamoyl-1h-pyrrol-1-ylamino)-5-oxopentanoate

https://huagongshe.com/reaction/218308

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant(2S)-5-(tert-butoxy)-2-{[(tert-butoxy)carbonyl]amino}-5-oxopentanoic acidHCID 6993432—
Reactant1-Amino-1H-pyrrole-2-carboxamideHCID 10419180—
SolventTetrahydrofuranHCID 8028—
Product(s)-Tert-butyl 4-(tert-butoxycarbonylamino)-5-(2-carbamoyl-1h-pyrrol-1-ylamino)-5-oxopentanoateHCID 5931369688.4%

Reaction Steps

A mixture of 1-amino-1H-pyrrole-2-carboxamide (1.00 g, 7.99 mmol) and (5)-5-tert-butoxy-2-(tert-butoxycarbonylamino)-5-oxopentanoic acid (2.91 g, 9.59 mmol) was dissolved in THF (80 mL). To this solution was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.84 g, 9.59 mmol). The reaction was stirred at rt for 1.5 h, then concentrated in vacuo. CH2Cl2 (150 mL) was added, and the reaction mixture was washed with water (2×150 mL). The organic layer was dried (MgSO4), filtered, and concentrated in vacuo. The compound was purified by silica gel flash chromatography (0-35% 90:10:1 [CH2Cl2/MeOH/conc NH4OH]/CH2Cl2) to give 10A (2.90 g, 85%). 10A had an analytical HPLC retention time=2.05 min (Waters XBridge 4.6×50 mm, 5-95% aqueous acetonitrile over 5 min containing 10 mM ammonium acetate) and a LC/MS M−−1=409.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198438B2
Source datasetuspto-grants-2012_06
ORD IDord-be6d40c4fbb0499d8687bc0569e704de
Source noteuspto-grants-2012_06