Cesium carbonate → HCID 10626061, compound

HRID 1456176Notes

Reaction equation

HRID 1456176 reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:13][C:12]3[CH:14]=[C:15]([O:18][CH3:19])[CH:16]=[CH:17][C:11]=3[C:10]=2[N:20]([C:24]2[CH:29]=[CH:28][C:27]([OH:30])=[CH:26][CH:25]=2)[C:21](=[O:23])[CH3:22])=[CH:5][CH:4]=1.C([O-])([O-])=O.[Cs+].[Cs+].Cl.Cl[CH2:39][CH2:40][N:41]1[CH2:46][CH2:45][CH2:44][CH2:43][CH2:42]1.CO.C(Cl)(Cl)Cl>CN(C=O)C.O>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[S:13][C:12]3[CH:14]=[C:15]([O:18][CH3:19])[CH:16]=[CH:17][C:11]=3[C:10]=2[N:20]([C:24]2[CH:25]=[CH:26][C:27]([O:30][CH2:39][CH2:40][N:41]3[CH2:46][CH2:45][CH2:44][CH2:43][CH2:42]3)=[CH:28][CH:29]=2)[C:21](=[O:23])[CH3:22])=[CH:5][CH:4]=1

Participants

7

Procedure

To a solution of 2-(4-methoxyphenyl)-3-[N-(4-hydroxyphenyl)acetamido]-6-methoxy-benzo[b]thiophene (1.31 g, 3.13 mmol) and Cs2CO3 (4.10 g, 12.50 mmol) in 15 mL of anhydrous DMF was added 2-chlorethylpiperidine hydrochloride (1.15 g, 6.26 mmol). The resulting mixture was stirred vigorously at room temperature for 5 h. The reaction mixture was diluted with 200 mL of H2O, and then extracted several times with EtOAc. The combined organic was then washed with H2O several times and then dried (Na2SO4), Concentration in vacuo provided an oil. Chromatography (1% CH3OH/CHCl3, SiO2) provided 1.49 g (90%) of 2-(4-methoxyphenyl-3-[N-[4-[2-(1-piperidinyl)ethoxy]phenyl]acetamido]-6-methoxybenzo[b]thiophene as an amber oil. 1H NMR (DMSO-d6) δ (doubling due to amide rotamers) 7.66-6.70 (m, 11 H), 3.93 (m, 2H) 3.78 and 3.58 (s, 6H), 2.8-2.30 (m, 6H), 2.01 and 1.78 (s, 3H), 1.52-1.11 (m, 6H). FD mass spec: 530. Anal. Calcd. for C31H34N2O4S: C, 70.16; H, 6.46; N, 5.28. Found: C, 70.33; H, 6.34; N, 5.35.

Workup

  1. extractionextracted several times with EtOAc
  2. washThe combined organic was then washed with H2O several times
  3. customdried
  4. concentration(Na2SO4), Concentration in vacuo
  5. customprovided an oil

Sources & evidence

ORD record
ord-d3edffb08bca45a5ae1e73f87a916a01
Source dataset
uspto-grants-1998_12
Patent number
US05843963

Reaction notes

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