Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1790216Generated: October 25, 2026

2-Pentanamine → (2-{[5-(1-Methyl-butylcarbamoyl)-thiophene-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/1790216

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PentanamineHCID 12246—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 58191955HCID 58191955—
SolventTetrahydrofuranHCID 8028—
Product(2-{[5-(1-Methyl-butylcarbamoyl)-thiophene-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl esterHCID 69055708—

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of 4.4 g (12.1 mmol) 5-(2-tert-butoxycarbonylamino-phenylcarbamoyl)-thiophene-2-carboxylic acid in 80 ml THF were added 2.2 g (13.6 mmol) carbonyldiimidazol. The reaction mixture was stirred at 45° C. for 1 h and then cooled to rt. After addition of 1.05 g (12 mmol) 2-pentylamine the reaction mixture was kept at rt for 12 h. The solvent was evaporated and the residue was dissolved in 150 ml CH2 Cl2. The solution was washed twice with 150 ml water each and dried over magnesium sulfate. The solvent was evaporated and the residue was washed with diethyl ether to yield (2-{[5-(1-methyl-butylcarbamoyl)-thiophene-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester as a white solid, mp. 183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071219B2
Source datasetuspto-grants-2006_07
ORD IDord-a2cea9a32b0044a881f3c9217467f865
Source noteuspto-grants-2006_07