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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113470Generated: October 26, 2026

Toluene-4-sulfonic acid 1-methyl-piperidin-3-ylmethyl ester → (4-Isopropyl-piperazin-1-yl)-[1-(1-methyl-piperidin-3-ylmethyl)-1H-indol-5-yl]-methanone

https://huagongshe.com/reaction/2113470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantToluene-4-sulfonic acid 1-methyl-piperidin-3-ylmethyl esterHCID 21184160—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantMethanone,1h-indol-5-yl[4-(1-methylethyl)-1-piperazinyl]-HCID 57752818—
SolventTetrahydrofuranHCID 8028—
Product(4-Isopropyl-piperazin-1-yl)-[1-(1-methyl-piperidin-3-ylmethyl)-1H-indol-5-yl]-methanoneHCID 2365233496.5%

Reaction Steps

A mixture of 1.06 g (3.9 mmol) (1H-indol-5-yl)-(4-isopropyl-piperazin-1-yl)-methanone (intermediate 1); 0.484 g (4.3 mmol) KOtBu and 1.33 g (4.7 mmol) toluene-4-sulfonic acid 1-methyl-piperidin-3-ylmethyl ester (intermediate 6) in 20 mL THF was shaken at 60° C. for 3 h. After evaporation of all volatiles a mixture ethyl acetate was added and washed with water. The organic phase was dried with MgSO4 and evaporated to dryness. The residue was purified by column chromatography on silica eluting with a solvent mixture formed from DCM, methanol NEt3. The combined product fractions were evaporated to yield 1.44 g (91%) of the title compound as light yellow gum. MS(m/e): 383.5 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432255B2
Source datasetuspto-grants-2008_10
ORD IDord-49b392f28f494bed8baf1f129c963479
Source noteuspto-grants-2008_10