Methanethiol → HCID 15457081, compound

HRID 992885Notes

Reaction equation

HRID 992885 reaction equation
Br[CH2:2][C:3]1[O:4][C:5]2[C:11]([Cl:12])=[CH:10][C:9]([F:13])=[C:8]([C:14]3[C:15](=[O:25])[N:16]([CH3:24])[C:17]([C:20]([F:23])([F:22])[F:21])=[CH:18][CH:19]=3)[C:6]=2[CH:7]=1.[CH3:26][SH:27].C(=O)([O-])[O-].[K+].[K+]>C1COCC1>[Cl:12][C:11]1[C:5]2[O:4][C:3]([CH2:2][S:27][CH3:26])=[CH:7][C:6]=2[C:8]([C:14]2[C:15](=[O:25])[N:16]([CH3:24])[C:17]([C:20]([F:21])([F:23])[F:22])=[CH:18][CH:19]=2)=[C:9]([F:13])[CH:10]=1

Participants

5

Procedure

0.31 g (0.71 mmol) of 3-(2-bromomethyl-7-chloro-5-fluorobenzofuran-4-yl)-1-methyl-6-trifluoromethyl-2-(1H)-pyridone was dissolved in 20 ml of THF, and 0.014 g (0.85 mmol) of a methanethiol 30% methanol solution and 0.12 g (0.85 mmol) of potassium carbonate were added thereto, followed by stirring at room temperature for 8 hours. THF was distilled off under reduced pressure. Then, the obtained residue was poured into water and extracted with ethyl acetate. After washing with water, the organic layer was dried over anhydrous magnesium sulfate. Ethyl acetate was distilled off under reduced pressure. Then, the obtained crude crystals were washed with n-hexane to obtain 0.28 g (yield: 98%) of the desired product.

Workup

  1. distillationTHF was distilled off under reduced pressure
  2. additionThen, the obtained residue was poured into water
  3. extractionextracted with ethyl acetate
  4. washAfter washing with water
  5. dry with materialthe organic layer was dried over anhydrous magnesium sulfate
  6. distillationEthyl acetate was distilled off under reduced pressure
  7. customThen, the obtained crude crystals
  8. washwere washed with n-hexane

Sources & evidence

ORD record
ord-19f4691be988437595f99c0c0f0a0fcf
Source dataset
uspto-grants-2002_10
Patent number
US06472348B1

Reaction notes

Loading…