HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 25060727, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3,6,6-trimethyl-6,7-dihydro-1H-indol-4(5H)-one | HCID 24820798 | — |
| Reactant | HCID 25059433 | HCID 25059433 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 25060727 | HCID 25060727 | 29% |
Reaction Steps
To 3,6,6,-trimethyl-1,5,6,7-tetrahydro-indol-4-one (0.3 g, 1.2 eq) in dimethylacetamide (50 mL) is added slowly sodium hydride (50.8 mg, 1.5 eq). The resulting mixture is stirred at RT for 0.5 h. To that 7-Fluoro-2-methyl-quinazolin-4-ylamine (0.25 g, 1 eq) is added and the mixture is stirred at 150° C. for overnight. The mixture is poured into sat'd NaHCO3 aq. solution (300 mL), and extracted by EtOAc (3×100 mL). The combined organic layers are dried over Na2SO4, filtered, concentrated. The crude product is purified by flash chromatography, eluted by 50% EtOAc in Hexane to EtOAc to give 1-(4-Amino-2-methyl-quinazolin-7-yl)-3,6,6-trimethyl-1,5,6,7-tetrahydro-indol-4-one (0.135 g, 29% yield). LC/MS m/z=335 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678803B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-4102dfdfdc0841688909cd34b6d1b5da |
| Source note | uspto-grants-2010_03 |