Propylamine → HCID 22270286, compound

HRID 1393901Notes

Reaction equation

HRID 1393901 reaction equation
Cl[CH2:2][C:3]1[N:7]([CH2:8][CH2:9][CH3:10])[C:6]2[CH:11]=[CH:12][C:13]([CH2:15][O:16][Si:17]([CH3:23])([CH3:22])[C:18]([CH3:21])([CH3:20])[CH3:19])=[CH:14][C:5]=2[N:4]=1.[CH2:24]([NH2:27])[CH2:25][CH3:26]>C(#N)C>[CH2:24]([NH:27][CH2:2][C:3]1[N:7]([CH2:8][CH2:9][CH3:10])[C:6]2[CH:11]=[CH:12][C:13]([CH2:15][O:16][Si:17]([CH3:23])([CH3:22])[C:18]([CH3:21])([CH3:20])[CH3:19])=[CH:14][C:5]=2[N:4]=1)[CH2:25][CH3:26]

Participants

4

Reactant 2

HCID 7852PropylamineHCID 22270285HCID 22270285, compound

Product 1

HCID 22270286HCID 22270286, compoundYield 99%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent

Procedure

A solution of 2.0 g (5.6 mmole) of 1-{[2-(chloromethyl)-1-propylbenzimidazol-5-yl]methoxy}-1,1,2,2-tetramethyl-1-silapropane in 20 mL of anhydrous acetonitrile is treated with 10 mL of propylamine for 16 hr at room temperature. The solvent is removed in vacuo and the residue is partitioned between 30 mL of ethyl acetate and 10 mL of 1 N NaOH. The ethyl acetate layer is dried over anhydrous Na2SO4 and solvent removed in vacuo to afford 2.1 g (99%) of propyl({1-propyl-5-[(1,1,2,2-tetramethyl-1-silapropoxy)methyl]benzimidazol-2-yl}methyl)amine.

Workup

  1. customThe solvent is removed in vacuo
  2. customthe residue is partitioned between 30 mL of ethyl acetate and 10 mL of 1 N NaOH
  3. dry with materialThe ethyl acetate layer is dried over anhydrous Na2SO4 and solvent
  4. customremoved in vacuo

Sources & evidence

ORD record
ord-a8c5628145b144b8a13ff80183dcf5e6
Source dataset
uspto-grants-2008_03
Patent number
US07348326B2

Reaction notes

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