돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 417953생성일: 2026년 10월 25일

Diisopropylethylamine → Piperidin-4-ylmethyl 4-(4-methylphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/417953

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1-(p-Tolyl)piperazine dihydrochlorideHCID 83112—
반응물(tert-Butoxycarbonyl)piperidin-4-ylmethyl 4-nitrophenyl carbonateHCID 66650794—
용매DimethylformamideHCID 6228—
생성물Piperidin-4-ylmethyl 4-(4-methylphenyl)piperazine-1-carboxylateHCID 4263525250.4%

반응 단계

(tert-Butoxycarbonyl)piperidin-4-ylmethyl 4-nitrophenyl carbonate (Intermediate 2; 3.80 g, 10.0 mmol) was dissolved in DMF (100 mL). DIPEA (6.10 mL, 35.0 mmol) and 4-(4-methylphenyl)piperazine dihydrochloride (2.49 g, 10.0 mmol) were added. The reaction mixture was stirred at room temperature for 4 hours and then concentrated in vacuo. The resulting residue was dissolved in EtOAc (300 mL) and washed with a 1 M aq Na2CO3 solution (6×200 mL), 10% citric acid solution (50 mL), brine (50 mL), dried (MgSO4) and concentrated in vacuo. The residue was dissolved in a mixture of DCM (100 mL) and TFA (25 mL), stirred for 48 hours and then concentrated in vacuo. The residue was purified by reverse phase column chromatography (gradient eluting with MeOH in water, with 1% formic acid in each solvent, 0-30%). The resulting residue was dissolved in DCM (70 mL) and stirred with solid K2CO3 for 20 minutes, filtered and concentrated in vacuo to give piperidin-4-ylmethyl 4-(4-methylphenyl)piperazine-1-carboxylate (1.60 g, 44.6%) as a pale yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093248B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-2ef148b727514ffd98f93fca5a2a73f1
출처 메모uspto-grants-2012_01