HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → HCID 178429867, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 25061240 | HCID 25061240 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178429867 | HCID 178429867 | 48% |
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 (0.035 g, 0.1 mmol), hydroxylamine (7 mg, 0.1 mmol) and triethylamine (0.01 mL, 0.1 mmol) in EtOH (2 mL) is placed in an oil bath at 100° C. and stirred for 2 days. The solvent is evaporated under reduced pressure, and the residue is purified using a Biotage column (0-20% MeOH/CH2Cl2) to afford 0.017 g (48%) of 1-amino-N-hydroxy-6-(3,6,6-trimethyl-4-oxo-4,5,6,7-tetrahydro-indol-1-yl)-isoquinoline-4-carboxamidine. LC/MS m/z=378 [M+H]+, RT=1.82 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678803B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-d14ff28330fe4bd3ad299dd844cda953 |
| Source note | uspto-grants-2010_03 |