Methyl iodide → 2-[1-[(4-Fluorophenyl)methyl]-1,2,4-triazol-3-yl]-3-hydroxy-9,9-dimethyl-6,7-dihydropyrimido[2,1-c][1,4]oxazin-4-one

HRID 390352노트

반응식

HRID 390352 반응식
C([O:8][C:9]1[C:18](=[O:19])[N:17]2[C:12]([C:13]([CH3:21])([CH3:20])[O:14][CH2:15][CH2:16]2)=[N:11][C:10]=1[C:22](=S)[NH2:23])C1C=CC=CC=1.CI.[F:27][C:28]1[CH:38]=[CH:37][C:31]([CH2:32][N:33]([CH:35]=O)[NH2:34])=[CH:30][CH:29]=1.C([O-])(O)=O.[Na+]>C(#N)C.CN(C=O)C>[F:27][C:28]1[CH:29]=[CH:30][C:31]([CH2:32][N:33]2[CH:35]=[N:23][C:22]([C:10]3[N:11]=[C:12]4[N:17]([C:18](=[O:19])[C:9]=3[OH:8])[CH2:16][CH2:15][O:14][C:13]4([CH3:20])[CH3:21])=[N:34]2)=[CH:37][CH:38]=1

참가 물질

7

반응물 4

HCID 6328Methyl iodideHCID 516892Sodium BicarbonateHCID 58458904N-(4-Fluorobenzyl)formohydrazideHCID 584589233-(Benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carbothioamide

생성물 1

HCID 1361639592-[1-[(4-Fluorophenyl)methyl]-1,2,4-triazol-3-yl]-3-hydroxy-9,9-dimethyl-6,7-dihydropyrimido[2,1-c][1,4]oxazin-4-one수율 53%

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 6342Acetonitrile용매

반응 조건

온도
40 °C

실험 절차

To a solution of 3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carbothioamide (0.042 g, 0.122 mmol, 1.0 equiv) in acetonitrile (1.2 mL) under a nitrogen atmosphere, was added MeI (0.038 mL, 0.61 mmol, 5 equiv). The reaction was heated at 40° C. (oil bath) for 1 h. The reaction was then cooled to ambient temperature and concentrated in vacuo. N-(4-Fluorobenzyl)formohydrazide (0.045 g, 0.268 mmol, 2.2 equiv) was then added to the residue followed by DMF (1.5 mL) and the solution was heated at 140° C. (oil bath). After stirring 1 h, the reaction was cooled to ambient temperature stirred 17 h. The reaction was added to a saturated aqueous solution of NaHCO3 and extracted with CH2Cl2 (×3). The combined CH2Cl2 extracts were dried (Na2SO4) and then concentrated in vacuo. The crude product was purified by reverse phase preparatory HPLC and trituration from ether to provide the title compound (0.024 g, 53% yield) as an off-white solid. 1H NMR (400 MHz, CDCl3) δ ppm 8.10 (s, 1H), 7.29-7.35 (m, 2H), 7.07-7.14 (m, 2H), 5.44 (s, 2H), 4.02-4.10 (m, 4H), 1.68 (s, 6H); LCMS (ES+, (M+H)+) m/z 372.20.

후처리

  1. temperatureThe reaction was then cooled to ambient temperature
  2. concentrationconcentrated in vacuo
  3. temperaturethe solution was heated at 140° C. (oil bath)
  4. temperaturethe reaction was cooled to ambient temperature
  5. stirringstirred 17 h
  6. extractionextracted with CH2Cl2 (×3)
  7. dry with materialThe combined CH2Cl2 extracts were dried (Na2SO4)
  8. concentrationconcentrated in vacuo
  9. customThe crude product was purified by reverse phase preparatory HPLC and trituration from ether

출처 및 근거

ORD 기록
ord-d638aa9ed2aa42b5bf42c595701e025c
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08383639B2

반응 노트

불러오는 중…