Methyl fluorosulfate → HCID 70634328, compound

HRID 442314Notes

Reaction equation

HRID 442314 reaction equation
[CH:1]([N-]C(C)C)(C)C.[Li+].[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([S:16][CH2:17][C:18]([NH:20][CH:21]2[C:45](=[O:46])[N:23]3[C:24]([C:29]([O:31][CH:32]([C:39]4[CH:44]=[CH:43][CH:42]=[CH:41][CH:40]=4)[C:33]4[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=4)=[O:30])=[C:25]([OH:28])[CH2:26][S:27][C@H:22]23)=[O:19])=[CH:12][CH:11]=1.FS(OC)(=O)=O>CN(P(N(C)C)(N(C)C)=O)C>[Cl:9][C:10]1[CH:15]=[CH:14][C:13]([S:16][CH2:17][C:18]([NH:20][CH:21]2[C:45](=[O:46])[N:23]3[C:24]([C:29]([O:31][CH:32]([C:39]4[CH:40]=[CH:41][CH:42]=[CH:43][CH:44]=4)[C:33]4[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=4)=[O:30])=[C:25]([O:28][CH3:1])[CH2:26][S:27][C@H:22]23)=[O:19])=[CH:12][CH:11]=1

Participants

5

Procedure

A solution of 60 mg. of lithium diisopropylamide in 10 cc. of HMPA is cooled to 0° C. and 260 mg. of diphenylmethyl 7-(4-chlorophenylthio)acetamido-3-hydroxy-3-cephem-4-carboxylate is added in one portion. After stirring the reaction mixture for 1 minute, 70 mg. of methyl fluorosulfonate is added, and stirring is continued for 30 minutes. The reaction mixture is poured into 50 cc. of ethyl acetate, washed with water, and dried. Removal of the solvent under reduced pressure provides diphenylmethyl 7-(4-chlorophenylthio)acetamido-3-methoxy-3-cephem-4-carboxylate.

Workup

  1. stirringstirring
  2. waitis continued for 30 minutes
  3. additionThe reaction mixture is poured into 50 cc
  4. washof ethyl acetate, washed with water
  5. customdried
  6. customRemoval of the solvent under reduced pressure

Sources & evidence

ORD record
ord-47c0f00db3ba45dca9a7455523aa33a5
Source dataset
uspto-grants-1977_08
Patent number
US04045435

Reaction notes

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