HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene-4-sulfonic acid 1-methyl-piperidin-3-ylmethyl ester | HCID 21184160 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | Methanone,1h-indol-5-yl[4-(1-methylethyl)-1-piperazinyl]- | HCID 57752818 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4-Isopropyl-piperazin-1-yl)-[1-(1-methyl-piperidin-3-ylmethyl)-1H-indol-5-yl]-methanone | HCID 23652334 | 96.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432255B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-49b392f28f494bed8baf1f129c963479 |
| Source note | uspto-grants-2008_10 |