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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1052913생성일: 2026년 10월 25일

Oxygen → (2R,4R)-5-(3'-Chlorobiphenyl-4-yl)-2-hydroxy-4-[(1-hydroxy-1H-[1,2,3]triazole-4-carbonyl)-amino]pentanoic Acid

https://huagongshe.com/reaction/1052913

반응식

참여 물질

역할이름HCID투입량
반응물OxygenHCID 977—
반응물Potassium CarbonateHCID 11430—
반응물DiisopropylethylamineHCID 81531—
반응물(3-Chlorophenyl)boronic acidHCID 2734323—
반응물O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphateHCID 42624899—
반응물1-Hydroxy-1H-1,2,3-triazole-4-carboxylic AcidHCID 53433104—
반응물(2R,4R)-4-amino-5-(4-bromophenyl)-2-hydroxypentanoic acid ethyl esterHCID 67969401—
용매EthanolHCID 702—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물(2R,4R)-5-(3'-Chlorobiphenyl-4-yl)-2-hydroxy-4-[(1-hydroxy-1H-[1,2,3]triazole-4-carbonyl)-amino]pentanoic AcidHCID 5737798920.5%

반응 단계

1-Hydroxy-1H-1,2,3-triazole-4-carboxylic acid (17.6 mg, 136 μmol) and HCTU (56.4 mg, 136 μmol) were combined in DMF and stirred for 5 minutes at room temperature. DIPEA (71.2 μl, 409 μmol) and (2R,4R)-4-amino-5-(4-bromophenyl)-2-hydroxypentanoic acid ethyl ester (43 mg, 140 μmol) were added and the resulting mixture was stirred for 10 minutes. The reaction mixture was evaporated under reduced pressure and purified (C18 reverse phase column). The purified material was combined with 3-chlorophenylboronic acid, pinacol ester (48.1 mg, 202 μmol), K2CO3 (41.8 mg, 302 μmol), EtOH (1 ml) and water (0.3 ml). Oxygen was removed (high vacuum) and SilicaCat®Pd(0) (0.09 mmol/g loading; 112 mg, 10.1 μmol) was quickly added under nitrogen. The mixture was microwaved at 100° C. for 20 minutes, then concentrated. The material was redissolved in AcOH and purified by preparative HPLC to yield the title compound (12 mg; purity 95%). MS m/z [M+H]+ calc'd for C20H19ClN4O5, 431.10. found 431.4.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09388145B2
출처 데이터셋uspto-grants-2016_07
ORD IDord-7dc7cf8831984f8f9ecf3943cc6c0aa2
출처 메모uspto-grants-2016_07