Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656112Generated: November 1, 2026

Water → 3-(1,1-Dioxidotetrahydro-2H-thiopyran-4-yl)-5-{5-[(methyloxy)methyl]-2-thienyl}-1H-indole-7-carboxamide

https://huagongshe.com/reaction/656112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13025550HCID 13025550—
Reactant3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-7-carboxamideHCID 59332711—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
Solvent1,4-DioxaneHCID 31275—
Product3-(1,1-Dioxidotetrahydro-2H-thiopyran-4-yl)-5-{5-[(methyloxy)methyl]-2-thienyl}-1H-indole-7-carboxamideHCID 5933258643%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-Bromo-5-[(methyloxy)methyl]thiophene (35 mg, 0.16 mmol), 3-(1,1-dioxidotetrahydro-2H-thiopyran-4-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-7-carboxamide (55 mg, 0.13 mmol) and K2CO3 (83 mg, 0.14 mmol) was taken up in 1,4-dioxane (3 mL) and water (1.5 mL) in a microwave vial. The mixture was degassed by bubbling argon through it for 5 min. PdCl2(dppf) (17 mg, 0.023 mmol) was added, and the reaction was heated in a microwave for 5 min at 100° C. The reaction mixture was concentrated, diluted in DMSO, and purified on a Gilson HPLC (NH4OH buffer), giving 18.2 mg (43%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071584B2
Source datasetuspto-grants-2011_12
ORD IDord-b5d605157b4a41c589c8489fa59be4b8
Source noteuspto-grants-2011_12