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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Pentanamine | HCID 12246 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 58191955 | HCID 58191955 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2-{[5-(1-Methyl-butylcarbamoyl)-thiophene-2-carbonyl]-amino}-phenyl)-carbamic acid tert-butyl ester | HCID 69055708 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07071219B2 |
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| Source dataset | uspto-grants-2006_07 |
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| ORD ID | ord-a2cea9a32b0044a881f3c9217467f865 |
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| Source note | uspto-grants-2006_07 |
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