HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 1-(aminomethyl)cyclopentanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4-Dichloro-5-nitropyrimidine | HCID 521266 | — |
| Reactant | Methyl1-[(cyclopentylamino)methyl]cyclopentane-1-carboxylate | HCID 68683992 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 1-(aminomethyl)cyclopentanecarboxylate | HCID 13285792 | — |
Reaction Steps
Methyl1-[(cyclopentylamino)methyl]cyclopentane-1-carboxylate (Intermediate 258; 1.60 g, 7.10 mmol), 2,4-dichloro-5-nitropyrimidine (Aldrich; 1.66 g, 8.52 mmol) and triethylamine (1.2 mL, 8.52 mmol) were stirred in acetonitrile (50 mL) for 4 hours. The reaction mixture was evaporated and the residue dissolved in DCM, washed with water, dried (MgSO4) and evaporated. The residue was purified on a silica column eluting with 1% methanol/DCM to yield the title compound as a yellow oil that crystallised on standing (945 mg, 35%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709471B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-d8121f9908d746bda69347704d412b5f |
| Source note | uspto-grants-2010_05 |