HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2086273Generated: October 31, 2026
Triethylsilane → 4-(6-Chloronaphthalene-2-sulfonyl)-1-[1-(4-pyridyl)-4-piperidinylamino]-2-piperazinone
https://huagongshe.com/reaction/2086273
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | 4-(6-Chloronaphthalene-2-sulfonyl)-1-[1-(4-pyridyl)-4-piperidinylideneamino]-2-piperazinone | HCID 69545716 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | 4-(6-Chloronaphthalene-2-sulfonyl)-1-[1-(4-pyridyl)-4-piperidinylamino]-2-piperazinone | HCID 17825410 | 73% |
Reaction Steps
A solution of 4-(6-chloronaphthalene-2-sulfonyl)-1-[1-(4-pyridyl)-4-piperidinylideneamino]-2-piperazinone (120 mg) in trifluoroacetic acid (1 ml) was combined with triethylsilane (60 mg) and stirred at 50° C. for 4 hours. The reaction mixture was concentrated and the residue was combined with an ice-cooled 1 N aqueous solution of sodium hydroxide, extracted with dichloromethane, dried and then concentrated. The residue obtained was purified by a column chromatography (dichloromethane: 10% aqueous ammonia-containing methanol=20:1) and crystallized from acetone to obtain the title compound (88 mg) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06723722B1 |
|---|
| Source dataset | uspto-grants-2004_04 |
|---|
| ORD ID | ord-4c92d443e2fd4e679d434cf5158119ab |
|---|
| Source note | uspto-grants-2004_04 |
|---|