Ethanol → HCID 71008224, compound

HRID 1025634Notes

Reaction equation

[C:1]([C:5]1[CH:6]=[C:7]2[C:12](=[C:13]([F:15])[CH:14]=1)[C:11](=[O:16])[N:10]([C:17]1[C:18]([CH2:41][OH:42])=[C:19]([N:23]3[C:27]4=[N:28][C:29]([C:32]5[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=5[Cl:38])=[CH:30][CH:31]=[C:26]4[C:25]([C:39]#[N:40])=[CH:24]3)[CH:20]=[CH:21][CH:22]=1)[N:9]=[CH:8]2)([CH3:4])([CH3:3])[CH3:2].C([OH:45])C>O>[C:1]([C:5]1[CH:6]=[C:7]2[C:12](=[C:13]([F:15])[CH:14]=1)[C:11](=[O:16])[N:10]([C:17]1[C:18]([CH2:41][OH:42])=[C:19]([N:23]3[C:27]4=[N:28][C:29]([C:32]5[CH:37]=[CH:36][CH:35]=[CH:34][C:33]=5[Cl:38])=[CH:30][CH:31]=[C:26]4[C:25]([C:39]([NH2:40])=[O:45])=[CH:24]3)[CH:20]=[CH:21][CH:22]=1)[N:9]=[CH:8]2)([CH3:4])([CH3:2])[CH3:3]

Participants

Conditions

Temperature: 45 °C

Procedure

In a 25 mL round-bottomed flask, 1-(3-(6-tert-butyl-8-fluoro-1-oxophthalazin-2(1H)-yl)-2-(hydroxymethyl)phenyl)-6-(2-chlorophenyl)-1H-pyrrolo[2,3-b]pyridine-3-carbonitrile (4 mg, 6.92 μmol) and [hydrogen bis(dimethylphosphinito-kP)]platinum (II) (29.7 μg, 0.0692 μmol, Eq: 0.01) were combined with Ethanol (853 μl) and Water (853 μl) to give a colorless solution. The reaction mixture was heated to 45° C. and stirred for 1 h, then concentrated in vacuo. Mixture was diluted with acetonitrile and water and filtered. The resultant filtrate is lyophalized to give 1-[3-(6-tert-Butyl-8-fluoro-1-oxo-1H-phthalazin-2-yl)-2-hydroxymethyl-phenyl]-6-(2-chloro-phenyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid amide (3.9 mg, 95%, [M+H]+ 596).

Workup

customto give a colorless solution
concentrationconcentrated in vacuo
additionMixture was diluted with acetonitrile and water
filtrationfiltered

Sources & evidence

ORD record: ord-52f632a330644601a7f2aeb5aac728bd
Source dataset: uspto-grants-2014_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08729078B2

Reaction notes

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