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Triethylamine → HCID 10051708, compound

HRID 1081900
Notes
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Reaction equation

HRID 1081900 reaction equation
[CH2:1]([C:4]1[N:8]([CH2:9][C:10]2[CH:15]=[CH:14][C:13]([C:16]3[C:17]([C:22]([O:24]C(C)(C)C)=[O:23])=[CH:18][CH:19]=[CH:20][CH:21]=3)=[CH:12][CH:11]=2)[C:7]2[CH:29]=[C:30](C(O)=O)[CH:31]=[CH:32][C:6]=2[N:5]=1)[CH2:2][CH3:3].[C:36]([N:43]1[CH:47]=[CH:46][N:45]=[CH:44]1)(N1C=CN=C1)=O.C(N(CC)CC)C.CN[C:57]1[CH:63]=CC=[CH:60][C:58]=1N>O1CCCC1>[CH2:1]([C:4]1[N:8]([CH2:9][C:10]2[CH:11]=[CH:12][C:13]([C:16]3[C:17]([C:22]([OH:24])=[O:23])=[CH:18][CH:19]=[CH:20][CH:21]=3)=[CH:14][CH:15]=2)[C:7]2[CH:29]=[C:30]([C:44]3[N:43]([CH3:36])[C:47]4[CH:63]=[CH:57][CH:58]=[CH:60][C:46]=4[N:45]=3)[CH:31]=[CH:32][C:6]=2[N:5]=1)[CH2:2][CH3:3]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 4

HCID 8471TriethylamineHCID 682631,1'-CarbonyldiimidazoleHCID 78498N-Methyl-o-phenylenediamineHCID 21479324HCID 21479324, compound

Product 1

HCID 10051708HCID 10051708, compound

Reagents, catalysts & solvents 1

HCID 8028
Tetrahydrofuran
Solvent

Procedure

A suspension of 940 mg (2.0 mMol) of tert.-butyl 4'-[(2-n-propyl-6-carboxy-benzimidazol-1-yl)-methyl]biphenyl-2-carboxylate and 320 mg (2.0 mMol) of carbonyldiimidazole in a solution of 1.0 ml of triethylamine in 30 ml of tetrahydrofuran is stirred for 30 minutes at ambient temperature, then 250 mg (2.0 mMol) of 2-methylaminoaniline are added and the mixture is stirred for a further 16 hours. It is then evaporated to dryness and the residue is refluxed in 20 ml of phosphorus oxychloride, with stirring, for 1 hour. The majority of the phosphorus oxychloride is then distilled off, the dark, greasy residue is decomposed with 30 ml of water, the strongly acidic suspension thus obtained is refluxed for about 1 hour, adjusted to pH 6 after cooling and then concentrated by evaporation. The crude product obtained is purified by column chromatography (120 g of silica gel, eluant:methylene chloride/methanol=15:1).

Workup

  1. stirringthe mixture is stirred for a further 16 hours
  2. customIt is then evaporated to dryness
  3. temperaturethe residue is refluxed in 20 ml of phosphorus oxychloride
  4. stirringwith stirring, for 1 hour
  5. distillationThe majority of the phosphorus oxychloride is then distilled off
  6. customthe strongly acidic suspension thus obtained
  7. temperatureis refluxed for about 1 hour
  8. temperatureafter cooling
  9. concentrationconcentrated by evaporation

Sources & evidence

ORD record
ord-c50f928605064fb5a99a9316124ae0b4
Source dataset
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05587393

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes