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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2410366생성일: 2026년 10월 24일

Diisopropylethylamine → Methyl 1-({4-[({4-[(trans-2-Hydroxycyclopentyl)oxy]-1,2-benzisoxazol-3-yl}oxy)methyl]piperidin-1-yl}methyl)cyclopentanecarboxylate

https://huagongshe.com/ko/reaction/2410366

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참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methyl 1-(iodomethyl)cyclopentanecarboxylateHCID 67231596—
반응물trans-2-{[3-(Piperidin-4-ylmethoxy)-1,2-benzisoxazol-4-yl]oxy}cyclopentanolHCID 69316225—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물Methyl 1-({4-[({4-[(trans-2-Hydroxycyclopentyl)oxy]-1,2-benzisoxazol-3-yl}oxy)methyl]piperidin-1-yl}methyl)cyclopentanecarboxylateHCID 6931898611%

반응 조건

온도120 °C

반응 단계

A mixture of trans-2-{[3-(piperidin-4-ylmethoxy)-1,2-benzisoxazol-4-yl]oxy}cyclopentanol (77 mg, 0.23 mmol, EXAMPLE 33, Step 2), methyl 1-(iodomethyl)cyclopentanecarboxylate (75 mg, 0.28 mmol, EXAMPLE 33, Step 1), and N,N-diisopropylethylamine (0.12 mL, 0.70 mmol) in N-methylpyrrolidone (3.0 mL) was heated at 120° C. for 14 h. The mixture was cooled to room temperature and the mixture was diluted with ethyl acetate and water. The mixture was extracted with ethyl acetate (30 mL×2) and washed with brine. The extracts were combined and dried over sodium sulfate and concentrated in vacuo to give a brown solid. The residual solid was purified by silica gel column chromatography (hexane/ethyl acetate 3:2) to give 12 mg (11%) of the title compound as a colorless viscous oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08816090B2
출처 데이터셋uspto-grants-2014_08
ORD IDord-8b5dfdba53364787aa62430ea025b484
출처 메모uspto-grants-2014_08