Diisopropylethylamine → HCID 178522500, compound

HRID 1367957Notes

Reaction equation

HRID 1367957 reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([C:31]([OH:33])=O)[C:12]2[NH:16][C:15]([NH:17]C(C3N=CC4C(C=3)=CC=CC=4)=O)=[N:14][C:13]=2[CH:30]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN(C(ON1N=NC2[CH:45]=[CH:46][CH:47]=[CH:48][C:43]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CC[N:60]([CH:64]([CH3:66])[CH3:65])[CH:61]([CH3:63])C.S(O)(O)(=O)=[O:68].[NH2:72][C:73]1[NH:74][CH:75]=[CH:76][N:77]=1>CN(C=O)C.[Cl-].[Na+].O>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([C:31](=[O:33])[NH:72][C:73]2[NH:74][CH:75]=[CH:76][N:77]=2)[C:12]2[NH:16][C:15]([NH:17][C:66]([C:64]3[N:60]=[CH:61][C:63]4[C:45]([CH:65]=3)=[CH:46][CH:47]=[CH:48][CH:43]=4)=[O:68])=[N:14][C:13]=2[CH:30]=1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Participants

7

Reactant 4

HCID 81531DiisopropylethylamineHCID 135136Bis(2-amino-1H-imidazole) sulphateHCID 2733084Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 178522501HCID 178522501, compound

Product 1

HCID 178522500HCID 178522500, compoundYield 80%

Reagents, catalysts & solvents 2

HCID 6228DimethylformamideSolventHCID 57417360Sodium chloride; waterSolvent

Procedure

300 mg (0.75 mmol) of 6-benzyloxy-2-[(isoquinoline-3-carbonyl)-amino]-3H-benzoimidazole-4-carboxylic acid and 600 mg (1.58 mmol) of HBTU were dissolved in 2.0 mL of DMF and 1.0 mL of DIEA and reacted with 390 mg (3.0 mmol) of 2-aminoimidazole sulfate as described in general procedure A. Upon completion, the reaction was diluted with brine. The resulting solid was filtered, washed with water and EtOAc, and dried under vacuum to produce 300 mg (80%) of isoquinoline-3-carboxylic acid [5-benzyloxy-7-(1H-imidazol-2-ylcarbamoyl)-1H-benzoimidazol-2-yl]-amide. LCMS: 505 (M+1)+.

Workup

  1. filtrationThe resulting solid was filtered
  2. washwashed with water and EtOAc
  3. customdried under vacuum

Sources & evidence

ORD record
ord-4d588e9d21204ff1b75f181a8842d47b
Source dataset
uspto-grants-2011_02
Patent number
US07893267B2

Reaction notes

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