HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490289Generated: October 29, 2026
Ammonium formate → 1-(3-Methyl-isoquinolin-5-yl)-3-pyrrolidin-3-yl urea
https://huagongshe.com/reaction/490289
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium formate | HCID 2723923 | — |
| Reactant | 1-(1-Benzyl-pyrrolidin-3-yl)-3-(3-methyl-isoquinolin-5-yl)urea | HCID 10428622 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(3-Methyl-isoquinolin-5-yl)-3-pyrrolidin-3-yl urea | HCID 68855745 | 69.4% |
Reaction Steps
A solution of (D3) (2.30 g, 6.40 mmol), ammonium formate (2.02 g, 32.10 mmol) and 10% palladium on carbon (1 g) in methanol (100 mL) was heated at 70° C. for 3 h, then cooled to 25° C. and filtered through Celite. Evaporation in vacuo gave an oil which was suspended in dichloromethane and washed with saturated sodium carbonate solution. The organic layer was removed, dried (Na2SO4), and the solvents evaporated in vacuo to give the title compound as a yellow oil (1.2 g). 1H NMR (CDCl3) δ: 2.05-2.20 (2H, m), 2.68 (3H, s), 2.85-2.95 (2H, m), 3.00-3.15 (2H, m), 4.35-4.45 (1H, m), 5.85-5.90 (1H, m), 7.40-7.50 (2H, m), 7.62 (1H, s), 7.72 (1H, d, J=8.2 Hz), 7.91 (1H, d, J=7.6 Hz), 9.14 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07528150B2 |
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| Source dataset | uspto-grants-2009_05 |
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| ORD ID | ord-2e7d56c0bcf74146a804d5c5f54f7776 |
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| Source note | uspto-grants-2009_05 |
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