HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → HCID 25061489, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 25061240 | HCID 25061240 | — |
| Solvent | Dimethylsulfoxide ethanol | HCID 22338741 | — |
| Product | HCID 25061489 | HCID 25061489 | 29% |
Reaction Steps
A suspension of 1-amino-6-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-indol-1-yl)-isoquinoline-4-carbonitrile (0.066 g, 0.19 mmol) in EtOH/DMSO (3:1, 2 mL) is treated with an aqueous solution of NaOH (1 M, 0.03 mL) and H2O2 (30%, 0.1 mL). The reaction mixture is stirred at RT for 2 h. The reaction mixture is treated with H2O (20 mL). The aqueous phase is extracted with EtOAc (2×). The combined organic layers are dried over MgSO4. The solvent is evaporated and the residue is dried under vacuum. Purification of the crude material using a Biotage column (0-20% MeOH/CH2Cl2) affords 0.02 g (29%) of 1-amino-6-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-indol-1-yl)-isoquinoline-4-carboxylic acid amide. LC/MS m/z=363 [M+H]+, RT=1.93 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678803B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-5b588bcc52f0420bae55aa77746cae76 |
| Source note | uspto-grants-2010_03 |