Sodium hydride → HCID 14529434, compound

HRID 363389Notes

Reaction equation

HRID 363389 reaction equation
[C:1]1([CH3:52])[CH:6]=[CH:5][C:4]([S:7]([NH:10][CH2:11][CH2:12][CH2:13][N:14]([S:42]([C:45]2[CH:50]=[CH:49][C:48]([CH3:51])=[CH:47][CH:46]=2)(=[O:44])=[O:43])[CH2:15][CH2:16][N:17]([S:32]([C:35]2[CH:40]=[CH:39][C:38]([CH3:41])=[CH:37][CH:36]=2)(=[O:34])=[O:33])[CH2:18][CH2:19][CH2:20][NH:21][S:22]([C:25]2[CH:30]=[CH:29][C:28]([CH3:31])=[CH:27][CH:26]=2)(=[O:24])=[O:23])(=[O:9])=[O:8])=[CH:3][CH:2]=1.[H-].[Na+]>CN(C=O)C>[C:28]1([CH3:31])[CH:29]=[CH:30][C:25]([S:22]([N:21]2[CH2:20][CH2:19][CH2:18][N:17]([S:32]([C:35]3[CH:40]=[CH:39][C:38]([CH3:41])=[CH:37][CH:36]=3)(=[O:33])=[O:34])[CH2:16][CH2:15][N:14]([S:42]([C:45]3[CH:46]=[CH:47][C:48]([CH3:51])=[CH:49][CH:50]=3)(=[O:44])=[O:43])[CH2:13][CH2:12][CH2:11][N:10]([S:7]([C:4]3[CH:5]=[CH:6][C:1]([CH3:52])=[CH:2][CH:3]=3)(=[O:8])=[O:9])[CH2:19][CH2:18][N:17]([S:32]([C:35]3[CH:36]=[CH:37][C:38]([CH3:41])=[CH:39][CH:40]=3)(=[O:34])=[O:33])[CH2:16][CH2:15]2)(=[O:24])=[O:23])=[CH:26][CH:27]=1

Participants

4

Reactant 2

HCID 24758Sodium hydrideHCID 3090848N,N′-1,2-Ethanediylbis[4-methyl-N-[3-[[(4-methylphenyl)sulfonyl]amino]propyl]benzenesulfonamide]

Product 1

HCID 14529434HCID 14529434, compoundYield 55%

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent2×

Conditions

Temperature
100 °C

Procedure

To a stirred solution of 1,5,8,12-tetra(p-toluenesulfonyl)-1,5,8,12-tetraazadodecane prepared as in Example 11A (36.9 g, 0.0467 mole) in anhydrous DMF (470 ml) was added sodium hydride (2.80 g-80% in mineral oil, 0.0933 mole) in portions under a dry nitrogen blanket. The resulting mixture was stirred for 30 minutes under a dry argon atmosphere. The solution was then heated to 100° C. and a solution of 3-(p-toluenesulfonyl)-3-azapentane-1,5-di-p-toluenesulfonate prepared as in Example 11B (26.5 g, 0.0467 mole) in anhydrous DMF (230 mole) was added dropwise over a 3 h period, maintaining the temperature at 100° C. After stirring the solution an additional 1 h at 100° C., the mixture was concentrated in vacuo to a volume of 400 ml. H2O (1.5 l) was slowly added at room temperature to crystallize the product. The resulting pale yellow solid was filtered, washed thoroughly with H2O and dried in vacuo. The crude product was purified by recrystallization from CH2Cl2 -hexane to give 26.3 g (55% yield) of the product as a white crystalline solid: mp 235.5°-6.5° C. (dec.); 1H NMR (CDCl3) δ 2.09 (quint, J=6.6 Hz, 4 H), 2.44 (s, 6 H), 2.45 (s, 6 H), 2.46 (s, 3 H), 3.04 (t, J=7.5 Hz, 4 H), 3.13 (t, J=7.1 Hz, 4 H), 3.23 (m, 8 H), 3.45 (m, 4 H), 7.33 (m, 10 H), 7.72 (m, 10 H).

Workup

  1. additionwas added dropwise over a 3 h period
  2. temperaturemaintaining the temperature at 100° C
  3. stirringAfter stirring the solution an additional 1 h at 100° C.
  4. concentrationthe mixture was concentrated in vacuo to a volume of 400 ml
  5. additionH2O (1.5 l) was slowly added at room temperature
  6. customto crystallize the product
  7. filtrationThe resulting pale yellow solid was filtered
  8. washwashed thoroughly with H2O
  9. customdried in vacuo
  10. customThe crude product was purified by recrystallization from CH2Cl2 -hexane

Sources & evidence

ORD record
ord-02386dd3c68445a28ae798e16448c71b
Source dataset
uspto-grants-1999_02
Patent number
US05874421

Reaction notes

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