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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419068생성일: 2026년 10월 26일

Diisopropylethylamine → 1,2,3,4-Tetrahydro-1,8-naphthyridine

https://huagongshe.com/reaction/419068

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물1,8-NaphthyridineHCID 136069—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물1,2,3,4-Tetrahydro-1,8-naphthyridineHCID 13047367—
반응물5-Chloro-3-(4-chloro-3-trifluoromethyl benzenesulfonylamino)-pyridine-2-carboxylic acidHCID 57942077—
생성물1,2,3,4-Tetrahydro-1,8-naphthyridineHCID 13047367—
생성물4-chloro-N-[5-chloro-2-(3,4-dihydro-2H-[1,8]naphthyridine-1-carbonyl)-pyridin-3-yl]-3-trifluoromethyl-benzenesulfonamideHCID 57942323—

반응 단계

5-Chloro-3-(4-chloro-3-(trifluoromethyl)phenylsulfonamido)picolinic acid (208 mg, 0.50 mmol), 1,2,3,4-tetrahydro-[1,8]naphthyridine [(135 mg, 1.0 mmol) 1,2,3,4-tetrahydro-[1,8]naphthyridine was prepared freshly from 1,8-napthyridine via hydrogenation over Pt2O], BOP (486 mg, 1.1 mmol), DIEA (185 mg, 1.4 mmol) were reacted according to the procedure D to provide the title compound. HPLC purification (20→90% gradient of MeCN-water) provided 4-chloro-N-[5-chloro-2-(3,4-dihydro-2H-[1,8]naphthyridine-1-carbonyl)-pyridin-3-yl]-3-trifluoromethyl-benzenesulfonamide: MS m/z: 531.0 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093247B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-9696dc3f1b6b40a9912ee1c1b98ad082
출처 메모uspto-grants-2012_01