Hydrochloric Acid → HCID 76285608, 화합물

HRID 572037노트

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HRID 572037 반응식
[CH2:1]([O:8][C@H:9]1[CH2:13][N:12]([C:14]([O:16]C(C)(C)C)=O)[C@H:11]([CH2:21]O)[CH2:10]1)[C:2]1C=CC=CC=1.Cl.O1CCOCC1.[OH:30][CH:31]([C:35]1[CH:40]=[CH:39][CH:38]=[C:37]([C:41]([F:44])([F:43])[F:42])[CH:36]=1)[C:32]([OH:34])=O.F[P-](F)(F)(F)(F)F.N1(OC(N(C)C)=[N+](C)C)[C:56]2[N:57]=[CH:58][CH:59]=[CH:60][C:55]=2[N:54]=N1.C[N:70]1CCO[CH2:72][CH2:71]1>CO>[CH:60]1([C:55]2[N:54]=[CH:2][C:1]([O:8][C@H:9]3[CH2:13][N:12]4[C:14](=[O:16])[CH2:72][CH2:71][N:70]([C:32](=[O:34])[CH:31]([OH:30])[C:35]5[CH:40]=[CH:39][CH:38]=[C:37]([C:41]([F:44])([F:43])[F:42])[CH:36]=5)[CH2:21][C@@H:11]4[CH2:10]3)=[N:57][CH:56]=2)[CH2:59][CH2:58]1

참가 물질

8

반응물 6

HCID 313Hydrochloric AcidHCID 79724-MethylmorpholineHCID 312751,4-DioxaneHCID 101658DL-2-(3-Trifluoromethyl)phenylglycollic acidHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 14821719HCID 14821719, 화합물

생성물 1

HCID 76285608HCID 76285608, 화합물

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

To a solution of the product from Example 28, Part F (90 mg, 0.232 mmol) in anhydrous methanol (3 mL) was added 4 M HCl in 1,4-dioxane (0.579 mL, 2.317 mmol). The resulting mixture was stirred at room temperature for 18 hours, and the volatiles were removed in vacuo. The residue was suspended in N,N-dimethylformamide (3 mL), 2-hydroxy-2-(3-(trifluoromethyl)phenyl)acetic acid (0.056 g, 0.255 mmol), O-(7-azabenzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphate (HATU, 0.106 g, 0.278 mmol), and N-methyl morpholine (0.117 g, 1.158 mmol) were added, and the resulting solution was stirred at room temperature for 16 hours. The mixture was partitioned between water and ethyl acetate. The organic extract was washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography on silica gel using a solvent gradient of 0-7% methanol in dichloromethane. The title compound was obtained as a colorless solid (0.065 g, 57% yield). 1H NMR (400 MHz, pyridine-d5, 90° C.) δ ppm 8.09-7.99 (m, 2H), 7.98 (d, J=1.4 Hz, 1H), 7.87-7.79 (m, 1H), 7.56 (d, J=1.3 Hz, 1H), 7.43 (t, J=7.8 Hz, 1H), 5.94-5.85 (m, 1H), 5.40 (t, J=4.1 Hz, 1H), 4.90-4.15 (m, 3H), 4.12 (d, J=13.5 Hz, 1H), 3.73 (dd, J=13.5, 4.3 Hz, 1H), 3.50-2.15 (m, 6H), 2.07-1.79 (m, 2H), 1.05-0.93 (m, 2H), 0.95-0.83 (m, 2H).); MS (ESI) m/z 491 (M+H)+.

후처리

  1. customthe volatiles were removed in vacuo
  2. stirringthe resulting solution was stirred at room temperature for 16 hours
  3. customThe mixture was partitioned between water and ethyl acetate
  4. extractionThe organic extract
  5. washwas washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe crude product was purified by column chromatography on silica gel using a solvent gradient of 0-7% methanol in dichloromethane

출처 및 근거

ORD 기록
ord-1a0598faff80408692790122d9cbf55f
출처 데이터셋
uspto-grants-2015_05
특허 번호
US09029361B2

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