HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → HCID 25060728, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2,4-Quinazolinediamine, 7-fluoro- | HCID 456221 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3,6,6-trimethyl-6,7-dihydro-1H-indol-4(5H)-one | HCID 24820798 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 25060728 | HCID 25060728 | 77.7% |
Reaction Steps
To 3,6,6,-trimethyl-1,5,6,7-tetrahydro-indol-4-one (0.41 g, 1.2 eq) in dimethylacetamide (50 mL) is added slowly sodium hydride (69.5 mg, 1.5 eq) and the resulting mixture is stirred at RT for 0.5 h. Then 7-Fluoro-quinazolin-2,4-diamine (0.342 g, 1 eq) is added and the mixture is stirred at 150° C. for overnight. The reaction mixture is poured into sat'd NaHCO3 aq. solution (300 mL), extracted by EtOAc (3×150 mL). The combined organic layers are dried over Na2SO4, filtered, concentrated. The crude product is purified by flash chromatography to give 1-(2,4-Diamino-quinazolin-7-yl)-3,6,6-trimethyl-1,5,6,7-tetrahydro-indol-4-one (0.5 g, 77.6% yield). LC/MS m/z=336 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07678803B2 |
| Source dataset | uspto-grants-2010_03 |
| ORD ID | ord-d41c172ba27049b7b69bd6efd3321997 |
| Source note | uspto-grants-2010_03 |