Water → HCID 15491481, compound

HRID 567819Notes

Reaction equation

FC(F)(F)C([N:5]([CH2:39][CH2:40][O:41][CH3:42])[CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([CH2:13][CH2:14][NH:15][C:16]2[C:21](=[O:22])[N:20]([CH2:23][C:24]([NH:26][CH2:27][C:28]3[CH:29]=[C:30]4[C:34](=[CH:35][CH:36]=3)[NH:33][CH:32]=[C:31]4[CH3:37])=[O:25])[C:19]([CH3:38])=[CH:18][N:17]=2)[CH:8]=1)=O.C(=O)([O-])[O-].[Na+].[Na+].O>CO>[CH3:42][O:41][CH2:40][CH2:39][NH:5][CH2:6][C:7]1[CH:8]=[C:9]([CH:10]=[CH:11][CH:12]=1)[CH2:13][CH2:14][NH:15][C:16]1[C:21](=[O:22])[N:20]([CH2:23][C:24]([NH:26][CH2:27][C:28]2[CH:29]=[C:30]3[C:34](=[CH:35][CH:36]=2)[NH:33][CH:32]=[C:31]3[CH3:37])=[O:25])[C:19]([CH3:38])=[CH:18][N:17]=1

Participants

Conditions

Temperature: 50 °C

Procedure

2,2,2-Trifluoro-N-(2-methoxyethyl)N-[3-(2-{[5-methyl-4-(2-{[(3-methyl-1H-indol-5-yl)methyl]amino}-2-oxoethyl)-3-oxo-3,4-dihydro-2 pyrazinyl]amino}ethyl)benzyl]acetamide (preperation 45) (110 mg, 0.18 mmol) was dissolved in methanol(15 ml) and sodium carbonate solution in water (1.5 ml, 0.765 m, 1.15 mmol) was added. The reaction mixture was stirred for 56 hrs, after which time the reaction was heated to 50° C. and sodium carbonate (1.5 ml, 1.15 mmol) was added. The mixture was heated for 18 hrs and then partitioned between ethyl acetate and water, the organic layer was washed with brine, dried over MgSO4 and the solvent evaporated under reduced pressure. The crude product was triturated with diethyl ether:methanol (1:1) to afford the title compound, 23 mg, (25%).

Workup

temperatureThe mixture was heated for 18 hrs
custompartitioned between ethyl acetate and water
washthe organic layer was washed with brine
dry with materialdried over MgSO4
customthe solvent evaporated under reduced pressure
customThe crude product was triturated with diethyl ether:methanol (1:1)

Sources & evidence

ORD record: ord-e334fbf1b04f4609ad450900d8068135
Source dataset: uspto-grants-2001_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06180627B2

Reaction notes

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