Ammonia → HCID 67274343, compound

HRID 1696734Notes

Reaction equation

HRID 1696734 reaction equation
[CH3:1][O:2][C:3]1[CH:15]=[CH:14][C:6]2[S:7][CH:8]=[C:9]([S:10](Cl)(=[O:12])=[O:11])[C:5]=2[CH:4]=1.[NH3:16]>C1COCC1>[CH3:1][O:2][C:3]1[CH:15]=[CH:14][C:6]2[S:7][CH:8]=[C:9]([S:10]([NH2:16])(=[O:12])=[O:11])[C:5]=2[CH:4]=1

Participants

4

Procedure

To a solution of 5-methoxy-benzo[b]thiophene-3-sulfonyl chloride(0.80 g, 3.08 mmol) in THF (20 mL) was added ammonia gas until saturation at ca. 10° C., then the flask was stoppered, and the reaction mixture was stirred at rt for 4 h. The reaction mixture was then quenched with water; the organic solvent was slowly evaporated under vacuum. The precipitate formed was filtered off, washed with water and dried over P2O5 under high vacuum to obtain the desired compound (0.64 g) as a yellowish solid. MS (ISN): m/e 239.4 (M−H)−

Workup

  1. customThe reaction mixture was then quenched with water
  2. customthe organic solvent was slowly evaporated under vacuum
  3. customThe precipitate formed
  4. filtrationwas filtered off
  5. washwashed with water
  6. dry with materialdried over P2O5 under high vacuum

Sources & evidence

ORD record
ord-42b899cb8bfa4a65858229f6ff80c191
Source dataset
uspto-grants-2012_04
Patent number
US08163778B2

Reaction notes

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