Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 854390생성일: 2026년 10월 27일
((Chloromethyl)sulphonyl)benzene → 1-Methyl-4-{5-nitro-6-[(phenylsulfonyl)methyl]pyridin-2-yl}piperazine
https://huagongshe.com/reaction/854390
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | ((Chloromethyl)sulphonyl)benzene | HCID 81625 | — |
| 반응물 | 1-Methyl-4-(5-nitropyridin-2-yl)piperazine | HCID 2764066 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 1-Methyl-4-{5-nitro-6-[(phenylsulfonyl)methyl]pyridin-2-yl}piperazine | HCID 58934069 | 85% |
반응 단계
A stirred solution of 1-methyl-4-(5-nitropyridin-2-yl)piperazine (1.10 g, 5.00 mmol) and chloromethylphenylsulfone (0.950 g, 5.00 mmol) in dry THF, under nitrogen, is cooled to −60° C., treated with 1.0 M KOtBu in THF (10.0 mL, 10.0 mmol), allowed to warm to −10° C. over a 1 h period, quenched with acetic acid, treated sequentially with water and saturated aqueous NaHCO3 and extracted with CH2Cl2. The combined extracts are washed sequentially with water and brine, dried over MgSO4 and concentrated in vacuo. The resultant residue is crystallized from EtOAc to give the title compound as a yellow solid, 1.60 g (85% yield), mp: 170°-172° C., identified by mass spectral and NMR analyses.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07259165B2 |
|---|
| 출처 데이터셋 | uspto-grants-2007_08 |
|---|
| ORD ID | ord-b2b1b7e7168c4801a901b747bde79773 |
|---|
| 출처 메모 | uspto-grants-2007_08 |
|---|