HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 25061241, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3,6,6-trimethyl-6,7-dihydro-1H-indol-4(5H)-one | HCID 24820798 | — |
| Reactant | HCID 25059694 | HCID 25059694 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 25061241 | HCID 25061241 | 27.2% |
Reaction Steps
To 3,6,6,-trimethyl-1,5,6,7-tetrahydro-indol-4-one (0.104 g, 1.2 eq) in dimethylacetamide (3 mL), sodium hydride (14.4 mg, 1.2 eq) is added slowly and stirred at RT for 0.5 h. Then 1-(1-amino-6-fluoro-isoquinolin-4-yl)-ethanone (0.1 g, 1 eq) is added and stirred at 150° C. overnight. The reaction mixture is poured into Sat'd NH4Cl aq. (200 mL), extracted by EtOAc (3×100 mL), dried over Na2SO4, filtered, concentrated to give a crude product. That is purified by Biotage chromatography, eluted by 50-100% EtOAc in Hexanes to give 1-(4-acetyl-1-amino-isoquinolin-6-yl)-3,6,6 trimethyl-1,5,6,7-tetrahydro-indol-4-one (48.1 mg, 27%). LC/MS m/z=362 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678803B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-870c4b1750f940df8a2135ef0dc4e287 |
| Source note | uspto-grants-2010_03 |