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Morpholine → HCID 57635415, 화합물

HRID 1971101
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HRID 1971101 반응식
BrC1N2CCN(C)CC2=[C:4]([C:12]([NH:14][C@@H:15](C(C)(C)C)[C:16](NC)=[O:17])=O)N=1.[CH3:24][C:25]([CH3:53])([CH3:52])[C@H:26]([NH:31][C:32]([C:34]1[N:35]=[C:36]([C:44]#[C:45][C:46]2C=CC=CC=2)[N:37]2[CH2:42][CH2:41][N:40]([CH3:43])[CH2:39][C:38]=12)=[O:33])[C:27]([NH:29][CH3:30])=[O:28].ClC/C=C/B(O)O.C([O-])([O-])=O.[K+].[K+].N1CCOCC1>O1CCOCC1.CCOC(C)=O.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.O>[CH3:24][C:25]([CH3:53])([CH3:52])[C@H:26]([NH:31][C:32]([C:34]1[N:35]=[C:36](/[CH:44]=[CH:45]/[CH2:46][N:14]2[CH2:12][CH2:4][O:17][CH2:16][CH2:15]2)[N:37]2[CH2:42][CH2:41][N:40]([CH3:43])[CH2:39][C:38]=12)=[O:33])[C:27]([NH:29][CH3:30])=[O:28]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

10

반응물 5

HCID 8083MorpholineHCID 11430Potassium CarbonateHCID 6080110B-[(1E)-3-Chloro-1-propen-1-yl]boronic acidHCID 57635127HCID 57635127, 화합물HCID 57635398HCID 57635398, 화합물

생성물 1

HCID 57635415HCID 57635415, 화합물수율 34%

시약·촉매·용매

4
HCID 178418397HCID 178418397, 화합물촉매HCID 962Water용매HCID 8857Ethyl Acetate용매HCID 312751,4-Dioxane용매

실험 절차

(S)-3-bromo-N-(3,3-dimethyl-1-(methylamino)-1-oxobutan-2-yl)-7-methyl-5,6,7,8-tetrahydroimidazo[1,5-a]pyrazine-1-carboxamide (Compound 203; 0.12 g, 0.31 mmol) was dissolved in dioxane (4 mL) and (E)-3-chloroprop-1-enylboronic acid (0.037 g, 0.31 mmol) was added, followed by K2CO3 (0.11 g, 0.82 mmol), morpholine (0.054 g, 0.66 mmol) and water (0.80 mL). The resulting mixture was degassed with nitrogen and Pd(PPh3)4 (0.019 g, 0.017 mmol) was added. The mixture was subjected to microwave irradiation at 160° C. for 20 min. The mixture was diluted with EtOAc, and filtered through celite. The organic layer was concentrated, washed with water, dried over anhydrous Na2SO4, filtered and concentrated again. The residue was purified by prep LC/MS using 5-95% gradient acetonitrile/water with 0.1% formic acid to provide Compound 286 (0.035 g, 34%) as a yellow solid. 1H-NMR (400 MHz, CDCl3) δ: 1.07 (s, 9H), 2.52 (s, 3H), 2.81 (d, 3H), 2.89 (t, 2H), 2.97 (m, 3H), 3.28 (s, 1H), 3.58 (d, 1H), 3.99 (m, 8H), 4.35 (d, 1H), 6.11 (m, 1H), 6.68 (m, 2H), 7.71 (m, 1H); LCMS (+ESI) m/z 433.3 [M+H]+.

후처리

  1. additionwas added
  2. customirradiation at 160° C. for 20 min
  3. filtrationfiltered through celite
  4. concentrationThe organic layer was concentrated
  5. washwashed with water
  6. dry with materialdried over anhydrous Na2SO4
  7. filtrationfiltered
  8. concentrationconcentrated again
  9. customThe residue was purified by prep LC/MS

출처 및 근거

ORD 기록
ord-b7796c6f95f24b018e7c91ab276c954a
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08431565B2

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