Ethanethiol → HCID 59676117, compound

HRID 1391696Notes

Reaction equation

HRID 1391696 reaction equation
C[O:2][C:3]1[CH:4]=[C:5]2[C:13](=[CH:14][CH:15]=1)[N:12]([CH3:16])[C:11]1[C:6]2=[CH:7][CH:8]=[C:9]2[N:19]([CH3:20])[N:18]=[CH:17][C:10]2=1.[Al+3].[Cl-].[Cl-].[Cl-].CCS.C([O-])(O)=O.[Na+]>C(Cl)Cl>[CH3:20][N:19]1[C:9]2=[CH:8][CH:7]=[C:6]3[C:11]([N:12]([CH3:16])[C:13]4[C:5]3=[CH:4][C:3]([OH:2])=[CH:15][CH:14]=4)=[C:10]2[CH:17]=[N:18]1

Participants

6

Reactant 4

HCID 6343EthanethiolHCID 516892Sodium BicarbonateHCID 6451240Aluminum(III) ChlorideHCID 59676069HCID 59676069, compound

Product 1

HCID 59676117HCID 59676117, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A mixture of 7-methoxy-3,10-dimethyl-3,10-dihydro-2,3,10-triaza-cyclopenta[a]fluorene (55 mg, 0.21 mmol), AlCl3 (0.84 mmol, 4.0 eq.) and EtSH (0.63 mmol, 3.0 eq.) in CH2Cl2 (2 mL) was stirred at room temperature for 16 hours. The reaction mixture was poured into cold saturated NaHCO3 solution, extracted with CH2Cl2, washed with brine and dried, concentrated to yield the crude product. The crude product was then purified by chromatography to yield the title compound as a white solid.

Workup

  1. extractionextracted with CH2Cl2
  2. washwashed with brine
  3. customdried
  4. concentrationconcentrated
  5. customto yield the crude product
  6. customThe crude product was then purified by chromatography

Sources & evidence

ORD record
ord-3ab3c653f674454e9fe5c9992f698ea1
Source dataset
uspto-grants-2008_03
Patent number
US07338973B2

Reaction notes

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