HCID 70147406, compound → HCID 178438986, compound

HRID 984482Notes

Reaction equation

HRID 984482 reaction equation
[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10][C:11]1[CH:16]=[CH:15][C:14](/[CH:17]=[CH:18]/[C:19]([N:21]2[CH2:26][CH2:25][CH2:24][CH:23]([C:27]3[N:28]=[N:29][N:30](COC)[N:31]=3)[CH2:22]2)=[O:20])=[CH:13][C:12]=1[N+:35]([O-:37])=[O:36])([CH3:3])[CH3:2]>C(O)(C(F)(F)F)=O>[CH:1]([C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[S:10][C:11]1[CH:16]=[CH:15][C:14](/[CH:17]=[CH:18]/[C:19]([N:21]2[CH2:26][CH2:25][CH2:24][CH:23]([C:27]3[NH:28][N:29]=[N:30][N:31]=3)[CH2:22]2)=[O:20])=[CH:13][C:12]=1[N+:35]([O-:37])=[O:36])([CH3:3])[CH3:2]

Participants

3

Procedure

The compound from Example 279 (75 mg, 0.14 mmol) was dissolved in 1 mL of neat TFA and left at ambient temperature for overnight. The reagent was then removed in vacuo and the residue was evaporated twice with benzene. The crude product was purified using Gilson Preparative HPLC as described in Example 38B to give the title compound as a light-yellow solid (50 mg, 72%); 1H NMR (CDCl3, 300 MHz) δ 1.17 (d, J=6.5 Hz, 6H), 1.25-1.39 (m, 1H), 1.69-1.81 (m, 1H), 2.09 (br s, 1H), 2.14-2.30 (m, 1H), 2.57-2.71 (m, 1H), 3.35-3.66 (m, 3H), 3.90-4.03 (m, 1H), 4.66-4.78 (m, 1H), 6.73 (d, J=8.7 Hz, 1H), 6.86 (d, J=15.3 Hz, 1H), 7.32 (dd, J=2.1, 6.9 Hz, 1H), 7.42 (dd, J=2.1, 8.7 Hz, 1H), 7.47-7.57 (m, 3H), 7.76 (d, J=15.3 Hz, 1H), 8.46 (d, J=2.1 Hz, 1H). MS (ESI+) (M+H)+ at m/z 479. Anal. Calcd for C24H26N6O3S.0.28H2O: C, 59.61; H, 5.54; N, 17.38. Found: C, 59.71; H, 5.44; N, 16.99.

Workup

  1. customThe reagent was then removed in vacuo
  2. customthe residue was evaporated twice with benzene
  3. customThe crude product was purified

Sources & evidence

ORD record
ord-48d7e11d857c42b3905a4f8c87f7c40e
Source dataset
uspto-grants-2005_03
Patent number
US06867203B2

Reaction notes

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