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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634143Generated: November 1, 2026

Water → 4-(6-(5-(5-(4-methoxybenzylamino)-1,3,4-thiadiazol-2-yl)-1-tosyl-1H-indol-3-yl)pyrazin-2-yl)-1-methylpiperazin-2-one

https://huagongshe.com/reaction/634143

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant1-Methylpiperazin-2-oneHCID 4399042—
Reactant5-(3-(6-chloropyrazin-2-yl)-1-tosyl-1H-indol-5-yl)-N-(4-methoxybenzyl)-1,3,4-thiadiazol-2-amineHCID 86725096—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product4-(6-(5-(5-(4-methoxybenzylamino)-1,3,4-thiadiazol-2-yl)-1-tosyl-1H-indol-3-yl)pyrazin-2-yl)-1-methylpiperazin-2-oneHCID 68328025—

Reaction Conditions

Temperature155 °C

Reaction Steps

To a solution of 5-(3-(6-chloropyrazin-2-yl)-1-tosyl-1H-indol-5-yl)-N-(4-methoxybenzyl)-1,3,4-thiadiazol-2-amine (100 mg, 0.166 mmol) in NMP (1 mL) was added 1-methylpiperazin-2-one (28.4 mg, 0.249 mmol) and Et3N (69.2 μL, 0.497 mmol). The reaction was stirred at 155° C. for 18 h, then cooled to RT. H2O was added and the resulting suspension was filtered to give the crude material. MS (ESI, pos. ion) m/z: 681 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321756B2
Source datasetuspto-grants-2016_04
ORD IDord-17b32183141d4e2bb48e1352e5131631
Source noteuspto-grants-2016_04