Hydrochloric Acid → HCID 178508417, compound

HRID 1707479Notes

Reaction equation

HRID 1707479 reaction equation
C1(C([O:14][C:15]([C:17]2[N:22]3[C:23](=[O:42])[C@@H:24]([NH:25][C:26](=[O:41])[CH2:27][C:28]4[N:29]=[C:30]([NH:33]C(OC(C)(C)C)=O)[S:31][CH:32]=4)[C@H:21]3[S:20][CH2:19][C:18]=2[S:43][CH:44](C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[S:45][C:46]2[N:47]=[N:48][NH:49][CH:50]=2)=[O:16])C2C=CC=CC=2)C=CC=CC=1.[Cl-].[Al+3].[Cl-].[Cl-].Cl>C1(OC)C=CC=CC=1.[N+](C)([O-])=O.O>[NH2:33][C:30]1[S:31][CH:32]=[C:28]([CH2:27][C:26]([NH:25][C@@H:24]2[C:23](=[O:42])[N:22]3[C:17]([C:15]([OH:16])=[O:14])=[C:18]([S:43][CH2:44][S:45][C:46]4[N:47]=[N:48][NH:49][CH:50]=4)[CH2:19][S:20][C@H:21]23)=[O:41])[N:29]=1

Participants

7

Procedure

To a solution of 7β-[2-(2-t-butoxycarbonylaminothiazol-4-yl)acetamido]-3-(trityl-1,2,3-triazol-4-ylthiomethylthio)-3-cephem-4-carboxylic acid diphenylmethyl ester (779 mg: 0.784 mMol.) in a mixture of anisole (3 ml) and nitromethane (12 ml) at -40° C. is added a solution of aluminum chloride (0.83 g: 6.24 mMol.) in anisole (3 ml), and the mixture is stirred at -30° to -40° C. for 50 minutes. The reaction mixture is mixed with 1N-hydrochloric acid (6.3 ml), diluted with water, washed with ethyl acetate, and concentrated under reduced pressure to remove the remaining organic solvents. The residual solution is subjected to the chromatography over styrene-divinylbenzene copolymer (methanol: water=4:1) and resulting powder is washed with ethyl acetate to give 7β-[2-(2-aminothiazol-4-yl)acetamido]-3-(1,2,3-triazol-4-ylthiomethylthio)-3-cephem-4-carboxylic acid (225 mg) as white powder. Yield: 59%.

Workup

  1. washwashed with ethyl acetate
  2. concentrationconcentrated under reduced pressure
  3. customto remove the remaining organic solvents
  4. customresulting powder
  5. washis washed with ethyl acetate

Sources & evidence

ORD record
ord-c7a698b356494f54928df3fcb650be61
Source dataset
uspto-grants-1994_10
Patent number
US05352792

Reaction notes

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