Acetic Acid → HCID 178473890, compound

HRID 81218Notes

Reaction equation

HRID 81218 reaction equation
[C:1]([OH:4])(=O)[CH3:2].C(N(CC)C(C)C)(C)C.CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[Cl:38][C:39]1[CH:40]=[C:41]([C:45]2[C:50]3[N:51]([CH2:63][C@H:64]4[CH2:69][CH2:68][C@H:67]([CH3:70])[CH2:66][CH2:65]4)[C:52]([N:54]4[CH2:59][CH2:58][NH:57][C@@H:56]5[CH2:60][CH2:61][CH2:62][C@@H:55]45)=[N:53][C:49]=3[CH:48]=[C:47]([C:71]#[N:72])[N:46]=2)[CH:42]=[N:43][CH:44]=1>CS(C)=O.CCOC(C)=O>[C:1]([N:57]1[CH2:58][CH2:59][N:54]([C:52]2[N:51]([CH2:63][C@H:64]3[CH2:69][CH2:68][C@H:67]([CH3:70])[CH2:66][CH2:65]3)[C:50]3[C:45]([C:41]4[CH:42]=[N:43][CH:44]=[C:39]([Cl:38])[CH:40]=4)=[N:46][C:47]([C:71]#[N:72])=[CH:48][C:49]=3[N:53]=2)[C@@H:55]2[CH2:62][CH2:61][CH2:60][C@@H:56]12)(=[O:4])[CH3:2]

Participants

7

Procedure

Acetic acid (60.7 mg, 1.01 mmol), N,N-diisopropylethylamine (174 mg, 1.348 mmol) and HATU (513 mg, 1.348 mmol) were added to 4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(4aR,7aR)-octahydro-1H-cyclopenta[b]pyrazin-1-yl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile (177 mg, 0.33 mmol) in DMSO (1.5 ml), and the mixture was stirred at room temperature overnight. The reaction was then diluted with EtOAc, washed with water and brine, dried over sodium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel, eluting with EtOAc/isohexane to give 2-[(4aR,7aR)-4-acetyloctahydro-1H-cyclopenta[b]pyrazin-1-yl]-4-(5-chloropyridin-3-yl)-3-[(trans-4-methylcyclohexyl)methyl]-3H-imidazo[4,5-c]pyridine-6-carbonitrile. MS ESI calc'd. for C29H34ClN7O [M+H]+ 532. found 532.

Workup

  1. washwashed with water and brine
  2. dry with materialdried over sodium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by column chromatography on silica gel
  6. washeluting with EtOAc/isohexane

Sources & evidence

ORD record
ord-67980d4443b44de38e9da6ec02d549af
Source dataset
uspto-grants-2014_09
Patent number
US08846657B2

Reaction notes

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