HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-tert-butylimino-N,N-diethyl-1-methyl-1,3,2lambda5-diazaphosphinan-2-amine → HCID 178454061, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-tert-butylimino-N,N-diethyl-1-methyl-1,3,2lambda5-diazaphosphinan-2-amine | HCID 19990018 | — |
| Reactant | 1-Aminoisoquinolin-6-ol | HCID 135753991 | — |
| Reactant | HCID 178418975 | HCID 178418975 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178454061 | HCID 178454061 | 7.8% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
A suspension of 1-amino-6-hydroxyisoquinoline (0.08 g, 0.5mmol), methane-sulfonic acid trans-4-tert-butoxycarbonylaminocyclohexyl ester (176 mg) and 2-tert-butylimino-2-diethylamino-1,3-dimethyl-perhydro-1,3,2-diazaphosphorine on polystyrene (270mg, ˜2.2 mmol/g loading) in acetonitrile (2ml) were heated at 120° C. over a period of 15 minutes using the microwave. The excess supported reagent was removed by filtration, washing with acetonitrile followed by methanol, and the filtrate evaporated to dryness under reduced pressure. Purification was achieved by prep-HPLC to give cis-[4-(1-aminoisoquinolin-6-yloxy)cyclohexyl]carbamic acid tert-butyl ester (14 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893088B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-9d1c99598d674130a6e7095968db9a33 |
| Source note | uspto-grants-2011_02 |