Hydrochloric Acid → HCID 178441499, compound

HRID 2292721Notes

Reaction equation

HRID 2292721 reaction equation
[CH2:1]([C:5]1[N:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[C:23]3[N:27](C(C4C=CC=CC=4)(C4C=CC=CC=4)C4C=CC=CC=4)[N:26]=[N:25][N:24]=3)=[CH:13][CH:12]=2)[C:8]2[CH:47]=[C:48]([N:51]3[C:56](=[O:57])[CH2:55][C:54]([CH3:59])([CH3:58])[CH2:53][C:52]3=[O:60])[CH:49]=[CH:50][C:7]=2[N:6]=1)[CH2:2][CH2:3][CH3:4].Cl>CO>[CH2:1]([C:5]1[N:9]([CH2:10][C:11]2[CH:16]=[CH:15][C:14]([C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][C:18]=3[C:23]3[NH:27][N:26]=[N:25][N:24]=3)=[CH:13][CH:12]=2)[C:8]2[CH:47]=[C:48]([N:51]3[C:52](=[O:60])[CH2:53][C:54]([CH3:59])([CH3:58])[CH2:55][C:56]3=[O:57])[CH:49]=[CH:50][C:7]=2[N:6]=1)[CH2:2][CH2:3][CH3:4]

Participants

4

Procedure

A solution of 400 mg (0.5 mMol) of 4'-[[2-n-butyl-6-(3,3-dimethylglutarimido)-benzimidazol-1-yl]-methyl]-2-(1-triphenylmethyl-tetrazol-5-yl)-biphenyl in 10 ml of methanol is mixed with 1.5 ml of methanolic hydrochloric acid and stirred for 2 hours at ambient temperature, then concentrated by evaporation, the residue is mixed with 15 ml of water and made alkaline with concentrated ammonia, whereupon the product goes into solution. By acidification with glacial acetic acid, the crude product is precipitated and then purified by column chromatography (150 g of silica gel; eluant: methylene chloride +5% ethanol).

Workup

  1. concentrationconcentrated by evaporation
  2. additionthe residue is mixed with 15 ml of water
  3. customBy acidification with glacial acetic acid, the crude product is precipitated
  4. custompurified by column chromatography (150 g of silica gel; eluant: methylene chloride +5% ethanol)

Sources & evidence

ORD record
ord-8140db43790c4630a05e83ec91a40d42
Source dataset
uspto-grants-1997_11
Patent number
US05684029

Reaction notes

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