HCID 178418361, compound → HCID 178451915, compound
Reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH:12]([C:13]3[CH:18]=[CH:17][C:16]([N+:19]([O-])=O)=[CH:15][CH:14]=3)[CH2:11][CH2:10][CH:9]2[C:22]2[CH:27]=[CH:26][C:25]([C:28]3[N:29]=[C:30]([C@@H:33]4[CH2:37][CH2:36][CH2:35][N:34]4[C:38]([O:40][C:41]([CH3:44])([CH3:43])[CH3:42])=[O:39])[NH:31][CH:32]=3)=[CH:24][CH:23]=2)=[CH:4][CH:3]=1.[H][H]>C(O)C.C1COCC1.[Pt](=O)=O>[NH2:19][C:16]1[CH:17]=[CH:18][C:13]([CH:12]2[N:8]([C:5]3[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=3)[CH:9]([C:22]3[CH:27]=[CH:26][C:25]([C:28]4[N:29]=[C:30]([C@@H:33]5[CH2:37][CH2:36][CH2:35][N:34]5[C:38]([O:40][C:41]([CH3:44])([CH3:43])[CH3:42])=[O:39])[NH:31][CH:32]=4)=[CH:24][CH:23]=3)[CH2:10][CH2:11]2)=[CH:14][CH:15]=1Participants
6
Procedure
Dissolved the product from Example 39F (300 mg, 0.502 mmol) in ethanol (5 mL) and THF (5 mL) then added platinum(IV) oxide (22.8 mg, 0.1 mmol) and a hydrogen balloon and stirred the solution at room temperature for 2.5 h. Solution was filtered through celite and washed with methanol (10 mL), then concentrated to give the title compound (285 mg, 100%) as a colorless semi-solid and a 1/1 mixture of stereoisomers.
Workup
- filtrationSolution was filtered through celite
- washwashed with methanol (10 mL)
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-7d6a44b39f59425181d5f4ee53850ff6
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09006387B2
Reaction notes
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