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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656096Generated: October 25, 2026

Potassium Carbonate → 5-[3-({[(1S)-1,2-Dimethylpropyl]amino}methyl)phenyl]-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxamide

https://huagongshe.com/reaction/656096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3-Formylphenylboronic acidHCID 2734356—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant1,2-Dimethylpropylamine, (S)-HCID 6999788—
Reactant5-Bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxamideHCID 59332757—
CatalystZincchlorideHCID 3007855—
CatalystHCID 178418397HCID 178418397—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product5-[3-({[(1S)-1,2-Dimethylpropyl]amino}methyl)phenyl]-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxamideHCID 5933262315.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 5-bromo-3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-1H-indole-7-carboxamide (80 mg, 0.216 mmol) in dioxane and water (4 mL/1 mL) was added (3-formylphenyl)boronic acid (45 mg), Pd(PPh3)4 (25 mg) and K2CO3 (104 mg). The reaction mixture was redissolved in DMSO (2 mL). To the resultant mixture zinc chloride (30 mg), NaCNBH3 (30 mg) and (2s)-3-methyl-2-butanamine (50 mg) were added. The mixture was heated to 100° C. for 30 minutes by microwave irradiation and purified by HPLC with TFA to afford the title compound (16 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071584B2
Source datasetuspto-grants-2011_12
ORD IDord-1cd909fa55e74deea38760edf410ee6c
Source noteuspto-grants-2011_12