Cyanogen Bromide → HCID 86585895, compound

HRID 2120420Notes

Reaction equation

HRID 2120420 reaction equation
[CH2:1]([CH:8]([NH:22][C:23]([C:25]1[CH:34]=[N:33][C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[N:26]=1)=[O:24])[CH:9]([OH:21])[CH2:10][CH:11]([C:18](=[NH:20])[NH2:19])[CH2:12][CH2:13][C:14]([F:17])([CH3:16])[CH3:15])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[N:35]#[C:36]Br>C(Cl)Cl>[C:36]([N:20]=[C:18]([NH2:19])[CH:11]([CH2:12][CH2:13][C:14]([F:17])([CH3:16])[CH3:15])[CH2:10][CH:9]([OH:21])[CH:8]([NH:22][C:23]([C:25]1[CH:34]=[N:33][C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[N:26]=1)=[O:24])[CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)#[N:35]

Participants

4

Reactant 2

HCID 10476Cyanogen BromideHCID 86585893HCID 86585893, compound

Product 1

HCID 86585895HCID 86585895, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a solution of 1.0 equivalents of quinoxaline-2-carboxylic acid (1-benzyl-4-carbamimidoyl-7-fluoro-2-hydroxy-7-methyl-octyl)-amide in methylene chloride is added 1.0 equivalents of cyanogen bromide. The reaction is stirred at ambient temperature for approximately 15 hours. After standard aqueous work-up and extraction, followed by concentration and silica gel chromatography the title compound is obtained.

Workup

  1. extractionAfter standard aqueous work-up and extraction
  2. concentrationfollowed by concentration and silica gel chromatography the title compound
  3. customis obtained

Sources & evidence

ORD record
ord-0952e7603a324641acc8f65c7775f005
Source dataset
uspto-grants-2004_02
Patent number
US06689886B2

Reaction notes

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