1,2-Dichloroethane → HCID 67451027, 화합물

HRID 869184노트

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HRID 869184 반응식
C(C[C:4]1[S:8][C:7]([C:9]2[N:14]=[N:13][C:12]([N:15]([CH2:23][C:24]3([C:28]4[C:33]([F:34])=[CH:32][CH:31]=[CH:30][N:29]=4)[CH2:27][CH2:26][CH2:25]3)C(=O)OC(C)(C)C)=[CH:11][CH:10]=2)=[N:6][CH:5]=1)#N.Cl.CN.C1C=CC2N(O)N=[N:44][C:42]=2C=1.C(Cl)CCl.[C:52]([O:55]CC)(=O)[CH3:53]>Cl.CN(C=O)C>[F:34][C:33]1[C:28]([C:24]2([CH2:23][NH:15][C:12]3[N:13]=[N:14][C:9]([C:7]4[S:8][C:4]([CH2:53][C:52]([NH:44][CH3:42])=[O:55])=[CH:5][N:6]=4)=[CH:10][CH:11]=3)[CH2:25][CH2:26][CH2:27]2)=[N:29][CH:30]=[CH:31][CH:32]=1

참가 물질

8

실험 절차

A solution of t-butyl 6-(5-(cyanomethyl)thiazol-2-yl)pyridazin-3-yl((1-(3-fluoropyridin-2-yl)cyclobutyl)methyl)carbamate (1 g, 2 mmol) in HCl (30 mL, conc) was heated to 105° C. in a microwave reactor and stirred for 15 min. The reaction was concentrated to give 900 mg (2.3 mmol) of a crude reddish solid. To this solid was added methylamine hydrochloride (183 mg, 2.7 mmol), HOBt (365 mg, 2.7 mmol), EDC (516 mg, 2.7 mmol), DMF (30 mL), and TEA (1.3 mL, 9 mmol). The reaction was stirred at rt overnight. The reaction was then poured into ethyl acetate (200 mL), washed with water (3×100 mL), and the organic layer was separated, dried over Na2SO4, filtered, concentrated, and recrystallized from EtOAc to give 408 mg of 2-(2-(6-((1-(3-Fluoropyridin-2-yl)cyclobutyl)methylamino)pyridazin-3-yl)thiazol-5-yl)-N-methylacetamide as a white solid (M+H=413.3).

후처리

  1. concentrationThe reaction was concentrated
  2. customto give 900 mg (2.3 mmol) of a crude reddish solid
  3. stirringThe reaction was stirred at rt overnight
  4. washwashed with water (3×100 mL)
  5. customthe organic layer was separated
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customrecrystallized from EtOAc

출처 및 근거

ORD 기록
ord-b7690d34ee8a46aa8723bfc402a457ae
출처 데이터셋
uspto-grants-2015_03
특허 번호
US08969346B2

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