Trimethylsilyl iodide → HCID 86762223, compound

HRID 338139Notes

Reaction equation

HRID 338139 reaction equation
[C:1]([NH:9][C:10]1[S:11][CH2:12][C@@H:13]2[CH2:18][N:17](C(OCC3C=CC=CC=3)=O)[CH2:16][C@:14]2([C:29]2[S:30][CH:31]=[CH:32][CH:33]=2)[N:15]=1)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.I[Si](C)(C)C>C(#N)C>[S:30]1[CH:31]=[CH:32][CH:33]=[C:29]1[C@:14]12[CH2:16][NH:17][CH2:18][C@H:13]1[CH2:12][S:11][C:10]([NH:9][C:1](=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[N:15]2

Participants

4

Procedure

A solution of benzyl (4aR,7aR)-2-benzamido-7a-(2-thienyl)-4,4a,5,7-tetrahydropyrrolo[3,4-d][1,3]thiazine-6-carboxylate (14 g, 29.3 mmol) in acetonitrile (210 mL) is treated with iodotrimethylsilane (7.53 mL, 52.7 mmol) at room temperature. The solution is stirred for 1 hour and the solvent is evaporated. The residue is quenched with 1 M hydrochloric acid and ethyl acetate and the resulting mixture is filtered through diatomaceous earth. The aqueous layer is separated, neutralized with 50% w/w aqueous solution of sodium hydroxide and extracted with ethyl acetate. The organic extracts are dried over sodium sulfate and concentrated to give the title compound (7.9 g, 78%). ES/MS (m/e): 344 (M+H).

Workup

  1. customthe solvent is evaporated
  2. customThe residue is quenched with 1 M hydrochloric acid and ethyl acetate
  3. filtrationthe resulting mixture is filtered through diatomaceous earth
  4. customThe aqueous layer is separated
  5. extractionextracted with ethyl acetate
  6. dry with materialThe organic extracts are dried over sodium sulfate
  7. concentrationconcentrated

Sources & evidence

ORD record
ord-ddfcdfc8262a4e0794de0ec59f1f3170
Source dataset
uspto-grants-2014_11
Patent number
US08889856B2

Reaction notes

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