Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanethiol | HCID 8012 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(4-Amino-5-fluoro-7-quinazolinyl)-1,5,6,7-tetrahydro-3,6,6-trimethyl-4H-indol-4-one | HCID 25061236 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 25061237 | HCID 25061237 | — |
Reaction Steps
In a small microwave vial with a stir bar, butanethiol (0.494 mmol, 44.56 mg) is dissolved in 3 mL DMF. To this solution is added NaH (60% suspension in mineral oil) (0.494 mmol, 20 mg) and the mixture is stirred at rt for 5 minutes and then 1-(4-Amino-5-fluoro-quinazolin-7-yl)-3,6,6-trimethyl-1,5,6,7-tetrahydro-indol-4-one (0.0988 mmol, 33.4 mg) is added. The reaction is sealed and placed in the microwave reactor where it is heated to 120° C. for 30 min. The reaction is cooled and quenched by pouring into 30 ml sat. NH4Cl aq. and extracted 3 times with 10 mL EtOAc. The combined organics are dried with Na2SO4, concentrated, and purified by silica gel chromatography on Biotage using a gradient of 0-20% MeOH in DCM. 1-(4-Amino-5-butylsulfanyl-quinazolin-7-yl)-3,6,6-trimethyl-1,5,6,7-tetrahydro-indol-4-one is isolated (22.1 mg, LC/MS m/z=409 [M+H]+) as a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07678803B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-23b5919b9e4e4b6b8f5e3056fcad3332 |
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| Source note | uspto-grants-2010_03 |
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