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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49835생성일: 2026년 10월 24일

Hydrochloric Acid → [1-(Pyridin-4-yl)piperidin-4-yl]methanamine

https://huagongshe.com/ko/reaction/49835

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물PhthalimideHCID 6809—
반응물TriphenylphosphineHCID 11776—
반응물Hydrazine hydrate (1:1)HCID 24654—
반응물ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
반응물(1-(Pyridin-4-YL)piperidin-4-YL)methanolHCID 11310048—
용매EthanolHCID 702—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물[1-(Pyridin-4-yl)piperidin-4-yl]methanamineHCID 1060774656.7%

반응 조건

온도75 °C

반응 단계

A solution of 1-(4-pyridyl)piperidine-4-methanol (5.87 g, 30.6 mmol), phthalimide (4.59 g, 31.2 mmol), and triphenylphosphine (8.10 g, 30.9 mmol) in 125 mL of THF at −5° C. was treated with a solution of diethyl azodicarboxylate (5.38 g, 30.9 mmol) in THF (40 mL). After 16 h, the mixture was poured into EtOAc and 1 N HCl. The aqueous layer was washed with EtOAc (2×), pH adjusted to 12 by addition of 5 N NaOH, and washed with EtOAc (3×). The combined organic extracts were dried (K2CO3) and concentrated, yielding 8.45 g (86%). The crude material (5.47 g, 17.0 mmol) was then treated with hydrazine hydrate (3.5 mL, 60.0 mmol) in EtOH (50 ML). The mixture was heated at 75° C. for 5 h, cooled, diluted with CH2Cl2 (100 mL), and cooled to 0° C. The solid was removed by filtration; and the filtrate was concentrated, yielding 3.32 g of the title compound which was used without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710057B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-dad19736bdea4fb78ee7e9065f930181
출처 메모uspto-grants-2004_03