Iodine → HCID 24860658, 화합물

HRID 251346

반응식

HRID 251346 반응식
Br[CH:2]1[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1.[Mg].II.[NH2:11][C:12]1[N:16]([C:17]2[CH:18]=[C:19]([CH:26]=[CH:27][C:28]=2[CH3:29])[C:20]([NH:22][CH:23]2[CH2:25][CH2:24]2)=[O:21])[CH:15]=[N:14][C:13]=1[C:30]#N.C1C[O:35]CC1>>[NH2:11][C:12]1[N:16]([C:17]2[CH:18]=[C:19]([CH:26]=[CH:27][C:28]=2[CH3:29])[C:20]([NH:22][CH:23]2[CH2:25][CH2:24]2)=[O:21])[CH:15]=[N:14][C:13]=1[C:30]([CH:2]1[CH2:7][CH2:6][O:5][CH2:4][CH2:3]1)=[O:35]

참가 물질

6

실험 절차

A solution of 4-bromo-tetrahydro-pyran (0.82g, 5 mmol) in dry THF (10 mL) was added dropwise to the suspension of magnesium (132 mg, 5.5 mmol) and iodine (25 mg) in dry THF (20 mL) at 50° C. under N2. The mixture was stirred for 30 min after addition at 50° C., then cooled to room temperature. Then a THF (10 mL) solution of 3-(5-amino-4-cyano-imidazol-1-yl)-N-cyclopropyl-4-methyl-benzamide (90 mg, 0.32 mmol) was added to the reaction mixture and it was stirred at room temperature for 3h then quenched with HCl (2N) and stirred at room temperature overnight. The pH of the solution was adjusted pH 8 with saturated aqueous K2CO3 was and it was extracted with EtOAc. The organic layer was washed by water and brine, dried over Na2SO4, and concentrated. The crude product was purified by column chromatography on silical gel (EtOAc˜EtOAc:MeOH:Et3N=100:10:1), and the product was obtained as a beige solid (35 mg, 30%). HPLC (4 minute gradient) tR=3.05 min; MS m/z 369.18 [M+H]+.

후처리

  1. additionafter addition at 50° C.
  2. customthen quenched with HCl (2N)
  3. stirringstirred at room temperature overnight
  4. extractionit was extracted with EtOAc
  5. washThe organic layer was washed by water and brine
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customThe crude product was purified by column chromatography on silical gel (EtOAc˜EtOAc:MeOH:Et3N=100:10:1)

출처 및 근거

ORD 기록
ord-1cf12a8550e84eff861857800313f34d
출처 데이터셋
uspto-grants-2011_01
특허 번호
US07863314B2

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