反応 #8434

ord-ed49fbd1fa8449b196577007bf5b1c3e

反応方程式

CN1CCN(c2ccc3[nH]ccc3c2)CC1
5-(4-Methylpiperazin-1-yl)-indole
O=S(=O)(Cl)c1ccccc1
benzenesulfonylchloride
[Na+].[OH-]
NaOH
CN1CCN(c2ccc3c(ccn3S(=O)(=O)c3ccccc3)c2)CC1
oil
収率 66.0%
CN1CCN(c2ccc3c(ccn3S(=O)(=O)c3ccccc3)c2)CC1
N-Benzenesulfonyl-5-(4-methylpiperazin-1-yl)-indole
収率 66.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The organic layer was separated
  2. 2
    その他dried
  3. 3
    濃縮concentrated
  4. 4
    その他to give the crude as an oil that
  5. 5
    その他was purified on a silica column
  6. 6
    濃縮The pure fractions were concentrated

実験手順

5-(4-Methylpiperazin-1-yl)-indole (215 mg, 1 mmol), benzenesulfonylchloride (265 mg, 1.5 mmol) and Aliquat 336 (10 mg) were dissolved in DCM (10 mL). Aqueous NaOH (20%, 2 mL) was added and the mixture was stirred vigorously for 6 h. The organic layer was separated, dried and concentrated to give the crude as an oil that was purified on a silica column using DCM and MeOH as eluent. The pure fractions were concentrated to give an oil (260 mg, 0.66 mmol) 1H NMR (CDCl3) δ 2.35 (3 H, s), 2.59 (4 H, t, J=5), 3.18 (4 H, t, J=5), 6.57 (1 H, d, J=4), 6.98–7.03 (2 H, m), 7.38–7.54 (4 H, m), 7.82–7.90 (3 H, m); MS (posES-FIA) 355.1345 M+; Purity (HPLC chromsil C18) >98%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07087750B2uspto-grants-2006_08