Ethyl Acetate → Tivantinib

HRID 2234878Notes

Reaction equation

HRID 2234878 reaction equation
[C:1]1([C@H:13]2[C@@H:17]([C:18]3[C:26]4[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=4)[NH:20][CH:19]=3)[C:16](=[O:27])[NH:15][C:14]2=[O:28])[C:11]2=[C:12]3[C:7](=[CH:8][CH:9]=[CH:10]2)[CH2:6][CH2:5][CH2:4][N:3]3[CH:2]=1.CC(C)([O-])C.[K+].C(OCC)(=O)C>C(O)(C)(C)C>[C:1]1([C@H:13]2[C@H:17]([C:18]3[C:26]4[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=4)[NH:20][CH:19]=3)[C:16](=[O:27])[NH:15][C:14]2=[O:28])[C:11]2=[C:12]3[C:7](=[CH:8][CH:9]=[CH:10]2)[CH2:6][CH2:5][CH2:4][N:3]3[CH:2]=1

Participants

5

Reactant 3

HCID 8857Ethyl AcetateHCID 11717641(+)-cis-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4(1H-indol-3-yl)pyrrolidine-2,5-dioneHCID 23665647Potassium tert-butoxide

Product 1

HCID 11494412TivantinibYield 73.2%

Reagents, catalysts & solvents 1

HCID 6386tert-ButanolSolvent

Procedure

A preparation of (±)-cis-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4(1H-indol-3-yl)pyrrolidine-2,5-dione (378 mg, 1.02 mmol) was heated to 50° C. in tert-butanol (10 ml) and potassium t-butoxide (11 mg, 98 μmol) for 16 hours. The mixture was poured into ethyl acetate (100 ml) and washed with water (100 ml). The organic layer was dried over anhydrous sodium sulfate and evaporated to dryness to give (±)-trans-3-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)-4(1H-indol-3-yl)pyrrolidine-2,5-dione as a tan powder (276 mg). 1H NMR (DMSO-d6) 400 MHz δ: 11.54(s, 1H), 11.03(s, 1H), 7.32-7.4(m, 4H), 7.17(d, 1H, J=7.2 Hz), 7.07(t, 1H, J=7.6 Hz), 6.96(t, 1H, J=7.6 Hz), 6.82-6.89(m, 2H), 4.5(dd, 2H, J=7.2 and 20 Hz), 4.07(t, 2H, J=5.2 Hz), 2.87(t, 2H, J=6 Hz), 2.08(m, 2H).

Workup

  1. washwashed with water (100 ml)
  2. dry with materialThe organic layer was dried over anhydrous sodium sulfate
  3. customevaporated to dryness

Sources & evidence

ORD record
ord-2890d06a58cc4361bed9dea400f10119
Source dataset
uspto-grants-2010_05
Patent number
US07713969B2

Reaction notes

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