Sodium Iodide → HCID 43509650, compound

HRID 646978Notes

Reaction equation

HRID 646978 reaction equation
[CH3:1][N:2]1[CH2:8][CH2:7][CH2:6][N:5]([CH2:9][CH2:10][CH2:11][CH2:12][O:13]C2C=C(C=CN=2)C#N)[CH2:4][CH2:3]1.CN1CCCNCC1.ClCCCCO.C([O-])([O-])=O.[K+].[K+].[Na+].[I-]>C(O)CCC.O>[CH3:1][N:2]1[CH2:8][CH2:7][CH2:6][N:5]([CH2:9][CH2:10][CH2:11][CH2:12][OH:13])[CH2:4][CH2:3]1

Participants

8

Conditions

Temperature
95 °C

Procedure

2-[4-(4-Methyl-[1,4]diazepan-1-yl)-butoxy]-isonicotinonitrile. To a solution of 1-methyl-[1,4]diazepane (21.3 g, 185 mmol, 2.0 equiv) and 4-chloro-butan-1-ol (10.0 g, 92.6 mmol, 1.0 equiv) in 1-butanol (200 mL) were added K2CO3 (38.0 g, 278 mmol, 3.0 equiv) and NaI (13.9 g, 92.6 mmol, 1.0 equiv). The mixture was warmed to 95° C. and stirred for 36 h. The mixture was then cooled to rt, diluted with water, and extracted with chloroform (3×100 mL). The combined extracts were washed with brine, dried (MgSO4), filtered, and concentrated. Purification by Method 2 afforded 9.3 g of 4-(4-methyl-[1,4]diazepan-1-yl)-butan-1-ol with a small unidentified impurity. A portion of the impure alcohol (5.0 g) was dissolved in DMF (50 mL) and cooled to 0° C. Sodium hydride (60% dispersion in oil, 1.29 g, 32.2 mmol, 1.2 equiv) was added. The mixture was warmed to rt, stirred for 1 h, and then re-cooled to 0° C. A solution of 2-chloro-isonicotinonitrile (3.72 g, 26.8 mmol, 1.0 equiv) in DMF (25 mL) was added dropwise. The mixture was stirred at rt for 18 h, then was diluted with water (25 mL) and satd. aq. NaHCO3 (100 mL), and was extracted with chloroform (3×100 mL). The combined extracts were washed with brine, dried (Na2SO4), filtered and concentrated. Purification by Method 2 afforded the title compound (1.0 g). MS (electrospray): mass calculated for C16H24N4O, 288.20. m/z found, 289.4 [M+H]+. 1H NMR (400 MHz, CDCl3): 8.28 (dd, J=4.4 Hz, 0.8 Hz, 1H), 7.05 (dd, J=3.9, 1.1 Hz, 1H) 6.96 (s, 1H), 4.33 (t, J=6.6 Hz, 2H), 2.75-2.68 (m, 4H), 2.65-2.57 (m, 4H), 2.56-2.49 (m, 2H), 2.35 (s, 3H), 1.84-1.74 (m, 4H), 1.66-1.55 (m, 2H).

Workup

  1. temperatureThe mixture was then cooled to rt
  2. extractionextracted with chloroform (3×100 mL)
  3. washThe combined extracts were washed with brine
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customPurification by Method 2

Sources & evidence

ORD record
ord-f7e2f072dce14e889ae264fcb11010c5
Source dataset
uspto-grants-2010_04
Patent number
US07705149B2

Reaction notes

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