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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241477Generated: November 3, 2026

Hydrochloric Acid → [2-(1,1-Dioxo-thiomorpholine-4-carbonyl)-1H-indol-5-yl]-(4-isopropyl-piperazin-1-yl)-methanone

https://huagongshe.com/reaction/2241477

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantThiomorpholine 1,1-dioxideHCID 6484228—
Reactant5-(4-isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acidHCID 68534120—
SolventDimethylformamideHCID 6228—
Product[2-(1,1-Dioxo-thiomorpholine-4-carbonyl)-1H-indol-5-yl]-(4-isopropyl-piperazin-1-yl)-methanoneHCID 6868120664%

Reaction Steps

To the solution of 0.20 g (0.57 mmol) 5-(4-isopropyl-piperazine-1-carbonyl)-1H-indole-2-carboxylic acid 1:1 hydrochloride in 2 mL N,N-dimethylformamide, 0.19 g (0.60 mmol) O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (commercially available), 82 mg (0.60 mmol) thiomorpholine 1,1-dioxide (commercially available) and 0.58 mL (0.44 g, 3.4 mmol) N,N-diisopropylethylamine were added. After 1 h the solution was poured on saturated aqueous sodium bicarbonate solution, the phases were separated and the aqueous phase was extracted three times with ethyl acetate. The combined organic layers were washed three times with water followed by brine, dried over magnesium sulfate, filtered and evaporated. The residue was flash-chromatographed twice on silica gel with dichloromethane:methanol:ammonia (12:1:0.1 v/v) as eluant to give 0.13 g (64%) of the desired compound as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723325B2
Source datasetuspto-grants-2010_05
ORD IDord-fb699952727e45468ff11a9678bd65e0
Source noteuspto-grants-2010_05