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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 518672생성일: 2026년 10월 26일

Acetonitrile → HCID 178457835, 화합물

https://huagongshe.com/reaction/518672

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참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물Thionyl ChlorideHCID 24386—
반응물2-(4-Piperidyl)-2-propanolHCID 5200321—
반응물HCID 178457837HCID 178457837—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물Ammonium HydroxideHCID 14923—
생성물HCID 178457835HCID 178457835180.1%

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온도0 °C

반응 단계

To a solution of cis-4-(5-(hydroxymethyl)-2-nitrophenylamino)-N-isopropylcyclohexanecarboxamide (3.75 g, 11.18 mmol) in DCM (127 mL) at 0° C. was added thionyl chloride (4.08 mL, 55.9 mmol) dropwise. The reaction was stirred at 0° C. for 3 hours and then at RT for 2 hours. The reaction was concentrated in vacuo and suspended in ACN and re-concentrated to remove residual thionyl chloride. The residue was resuspended in ACN (102 mL, 11.18 mmol), cooled to 0° C., and to it was added 2-(piperidin-4-yl)propan-2-ol (5.60 g, 39.1 mmol). The reaction was stirred at RT overnight. The mixture was filtered, and the filtrate concentrated in vacuo. The residual material was purified via silica gel chromatography, eluting with 90:10:1 DCM:MeOH:NH4OH to provide cis-4-(5-((4-(2-hydroxypropan-2-yl)piperidin-1-yl)methyl)-2-nitrophenylamino)-N-isopropylcyclohexanecarboxamide (4.64 g, 10.07 mmol, 90% yield) as an orange solid. MS m/z=461.4 [M+H], calc 460.61 for C25H40N4O4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115127B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-c3cf6107a4c94976af1aae35b8a24af8
출처 메모uspto-grants-2015_08