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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 382934생성일: 2026년 10월 25일

Water → Phthalazine

https://huagongshe.com/reaction/382934

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물(1-Methyl-1H-1,2,4-triazol-3-yl)methanolHCID 10351670—
반응물6,10-Bis[(2-pyridyl)methyloxy]-3-(5-methylisoxazol-3-yl)-1,2,4-triazolo[3,4-a]phthalazineHCID 18361769—
용매DimethylformamideHCID 6228—
생성물PhthalazineHCID 920779.7%

반응 단계

Lithium hexamethyldisilazide (1.0M solution in hexane) (0.22 ml, 1.10 mmol) was added to stirred solution of 3-hydroxymethyl-1-methyl-1,2,4-triazole (90 mg, 0.79 mmol) prepared using the conditions of Itoh and Okongi, EP-A-421210) in N,N-dimethylformamide (10 ml) at −10° C. under nitrogen, and the mixture stirred for 0.25 h. After this time, Intermediate 6 (100 mg, 0.53 mmol) was added and the mixture stirred at −10° C. for 0.5 h and then room temperature overnight. Water was added to the reaction mixture and the resulting precipitate filtered off and recrystallised from dichloromethane/ethyl acetate to give the title-phthalazine (55 mg, 27%), mp 221-223° C.; 1H NMR (360 MHz, CDCl3) δ 1.54 (3H, t, J=10.2 Hz; CH3), 3.96 (3H, s, CH3), 4.47 (2H, q, J=10.2 Hz, CH2), 5.71 (2H, s, CH2), 6.26 (1H, s, Ar—H), 7.79 (1H, m, Ar—H), 7.94 (1H, m, Ar—H), 8.08 (1H, s, Ar—H), 8.25 (1H, d, J=11.0 Hz, Ar—H), 8.70 (1H, d, J=8.1 Hz, Ar—H); MS (ES+) m/e 393 [MH]+; Anal. Found. C, 54.87; H, 3.91; N, 28.27; C18H16N8O3 requires C, 55.09; H, 4.11; N, 28.55%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06310203B1
출처 데이터셋uspto-grants-2001_10
ORD IDord-c28531e728fd4cc7b1aca5eb1343375e
출처 메모uspto-grants-2001_10