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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25246생성일: 2026년 10월 25일

Triethylamine → HCID 178480341, 화합물

https://huagongshe.com/reaction/25246

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Pseudosaccharin chlorideHCID 64783—
반응물2-amino-N-(-4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexylpropionamide bis hydrochloride saltHCID 22566339—
용매AcetonitrileHCID 6342—
생성물HCID 178480341HCID 17848034149.4%

반응 단계

A suspension of 3-chloro-benzo[d]isothiazole 1,1-dioxide (300 mg, 1.49 mmol) and 2-amino-N-(-4-cyano-1-methyl-piperidin-4-yl)-3-cyclohexylpropionamide bis hydrochloride salt (500 mg, 1.37 mmol) was prepared in 5.5 mL of acetonitrile. Triethylamine (575 μL, 4.10 mmol) was added and the reaction mixture was stirred at room temperature for 1 day. The suspension was filtered to remove triethylamine hydrochloride and the filtrate was concentrated. The resulting residue was chromatographed over 50 g of flash silica using dichloromethane/methanol 9:1 as the eluant to provide the desired product as a light yellow solid (310 mg, 49%). 1H NMR (400 MHz, CDCl3) δ 0.25-0.45 (m, 1H), 0.65-0.85 (m, 2H), 0.95-1.10 (m, 2H), 1.30-1.60 (m, 7H), 1.75-1.85 (m, 2H), 1.85-2.2 (m, 2H), 2.31 (s, 3H), 2.35-2.50 (m, 3H), 2.65-2.80 (m, 2H), 4.60-4.70 (m, 1H), 7.35-7.50 (m, 2H), 7.58 (t, J=7.3, 1H), 7.78 (d, J=7.7 Hz, 1H), 7.81 (br s, 1H), 8.91 (br s, 1H). MS, m/z 458=M+1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858623B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-f3a049b0a1db4f9f88c6f52ab4e569f9
출처 메모uspto-grants-2005_02