HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Aminoisoquinoline → 1-Cyclopentyl-3-(isoquinolin-5-yl)urea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Aminoisoquinoline | HCID 70766 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Cyclopentyl Isocyanate | HCID 643500 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-Cyclopentyl-3-(isoquinolin-5-yl)urea | HCID 47193107 | — |
Reaction Steps
To isoquinolin-5-amine (0.23 g, 1.595 mmol) in DCM (5 mL) was added DIEA (0.557 mL, 3.19 mmol) and isocyanatocyclopentane (0.180 mL, 1.595 mmol). After 24 h, the reaction was quenched with H2O (15 mL) and extracted with EtOAc (3×30 mL). The combined organic layers were washed with brine (10 mL) and dried (MgSO4). The impure yellow solid was collected and was carried onto the next step. MS (ESI) m/z: 256 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447110B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-1795619309db438199d1eeb3372fdb91 |
| Source note | uspto-grants-2016_09 |