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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7903생성일: 2026년 10월 23일

2-Hydrazinopyridine → 1-(3,3-Dimethyl-2-oxo-pentanoyl)-pyrrolidine-2-carboxylic acid N'-pyridine-2-yl-hydrazide

https://huagongshe.com/ko/reaction/7903

반응식

참여 물질

역할이름HCID투입량
반응물2-HydrazinopyridineHCID 78645—
반응물DiisopropylethylamineHCID 81531—
반응물Methyl L-prolinateHCID 853477—
반응물PyBroPHCID 2733179—
반응물Gpi-1485HCID 9837656—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물1-(3,3-Dimethyl-2-oxo-pentanoyl)-pyrrolidine-2-carboxylic acid N'-pyridine-2-yl-hydrazideHCID 10268491—

반응 단계

A mixture of (2S)-1-(1,2-dioxo-3,3-dimethylpentyl)-2-pyrrolidine-carboxylic acid (482 mg, 2 mmol), prepared from L-proline methyl ester according to the procedure described in WO 96/40633, 2-hydrazinopyridine (364 mg, 2 mmol), PyBrop (932 mg, 2 mmol), DMAP (4-dimethyaminopyridine, 122 mg) and DIEA (4 mL) in THF (dry, 50 mL) was stirred at room temperature for 24 h. Water and ethyl acetate were added. The organic phase was washed with ammonium chloride solution, followed by brine, and dried with MgSO4. Column chromatography (silica gel, ethyl acetate:methanol=10:0.5) gave a colorless oil; 490 mg (74%); MS (m/z) 333 (M+1); 1H NMR (d6-DMSO) δ0.85 (t, J=8 Hz, 3 H), 1.21 (s, 3 H), 1.23 (s, 3 H), 1.7 (m, 2 H), 1.90 (m, 1 H), 2.10 (m, 2 H), 2.35 (m, 1 H), 3.49 (t, J=8 Hz, 2 H), 4.62 (m, 1 H), 6.76 (m, 2 H), 7.51 (t, J=6 Hz, 1 H), 8.14 (d, J=6 Hz, 1 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07087628B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-bd4a17db7fd44b94ad9c395a089d4e4a
출처 메모uspto-grants-2006_08