1,2-Dihydro-4-(6-iodohexyloxy)-1,2-dioxonaphthalene → 2'-[4-[6-(1,2-Dihydro-1,2-dioxo-naphth-4-yl)oxyhexyl]oxyphenyl]-5-(4-methylpiperazin-1-yl)-2,5'-bi-1h-benzimidazole

HRID 479980Notes

Reaction equation

HRID 479980 reaction equation
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([C:8]2[CH:13]=[CH:12][C:11]3[N:14]=[C:15]([C:17]4[CH:22]=[CH:21][C:20]5[NH:23][C:24]([NH:32][C:19]=5[CH:18]=4)=[C:25]4[CH:31]=[CH:30][C:28](=[O:29])[CH:27]=[CH:26]4)[NH:16][C:10]=3[CH:9]=2)[CH2:4][CH2:3]1.I[CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH2:39][O:40][C:41]1[C:50]2[C:45](=[CH:46][CH:47]=[CH:48][CH:49]=2)[C:44](=[O:51])[C:43](=[O:52])[CH:42]=1>CO.CN(C=O)C.O>[O:51]=[C:44]1[C:45]2[C:50](=[CH:49][CH:48]=[CH:47][CH:46]=2)[C:41]([O:40][CH2:39][CH2:38][CH2:37][CH2:36][CH2:35][CH2:34][O:29][C:28]2[CH:30]=[CH:31][C:25]([C:24]3[NH:23][C:20]4[CH:21]=[CH:22][C:17]([C:15]5[NH:14][C:11]6[CH:12]=[CH:13][C:8]([N:5]7[CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]7)=[CH:9][C:10]=6[N:16]=5)=[CH:18][C:19]=4[N:32]=3)=[CH:26][CH:27]=2)=[CH:42][C:43]1=[O:52]

Participants

6

Reactant 2

HCID 226477941,2-Dihydro-4-(6-iodohexyloxy)-1,2-dioxonaphthaleneHCID 178480630HCID 178480630, compound

Product 1

HCID 1784806372'-[4-[6-(1,2-Dihydro-1,2-dioxo-naphth-4-yl)oxyhexyl]oxyphenyl]-5-(4-methylpiperazin-1-yl)-2,5'-bi-1h-benzimidazoleYield 30.1%

Reagents, catalysts & solvents 3

HCID 887MethanolSolvent2×HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

Hoechst 33258 (3.0 g, 5 mmol) was dissolved in a hot mixture of isopropanol-water (24 mL/12 mL) and neutralized with ammonium hydroxide (3 mL). The precipitate was filtered, triturated with Et2O and dried in vacuo to obtain the free base of bisbenzimidazole. A 1.0 M solution of B4NOH in MeOH (0.6 mL, 0.6 mmol) was added to the solution of bisbenzimidazole (1.635 g, 3.85 mmol) in MeOH (30 mL), stirred for 15 min and concentrated to dryness in vacuo. Iodonaphthoquinone 505 (1.485 g, 3.87 mmol) in DMF (30 mL) was added to the teirabutyl ammonium salt and the mixture was stirred for 48 h. The reaction mixture was suspended in H2O, the crude product was filtered, washed with H2O, dried and purified by flash chromatography (MeOH/CHCl3 1:9, 1:5) to afford 514 as a yellow solid (790 mg, 30%). 1H NMR (CDCl3/MeOH-d4) 8.21 (s, 1H), 8.09 (d, J=7.6 Hz, 1H), 8.05 (d, J=8.7 Hz, 2H), 7.85-7.95 (m, 2H), 7.48-7.75 (m, 4H), 7.14 (bs, 1H), 7.10-6.98 (m 3H), 4.21 (t, J=6.3 Hz, 2H), 4.08 (t, J=6.2 Hz, 2H), 2.65-2.75 (m, 4H), 2.40 (s, 3H), 1.80-2.15 (m, 4H), 1.60-1.75 (m, 4H). MS (LSIMS, 3-NBA) 725.2 (M++1).

Workup

  1. concentrationconcentrated to dryness in vacuo
  2. stirringthe mixture was stirred for 48 h
  3. filtrationthe crude product was filtered
  4. washwashed with H2O
  5. customdried
  6. custompurified by flash chromatography (MeOH/CHCl3 1:9, 1:5)

Sources & evidence

ORD record
ord-e51bb1f1776d4cfd9f400379d43b05e5
Source dataset
uspto-grants-2003_11
Patent number
US06649587B1

Reaction notes

Loading…