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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | (2S)-5-(tert-butoxy)-2-{[(tert-butoxy)carbonyl]amino}-5-oxopentanoic acid | HCID 6993432 | — |
| Reactant | 1-Amino-1H-pyrrole-2-carboxamide | HCID 10419180 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (s)-Tert-butyl 4-(tert-butoxycarbonylamino)-5-(2-carbamoyl-1h-pyrrol-1-ylamino)-5-oxopentanoate | HCID 59313696 | 88.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08198438B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-be6d40c4fbb0499d8687bc0569e704de |
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| Source note | uspto-grants-2012_06 |
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