Sodium Hydroxide → N-(1H-benzoimidazol-2-ylmethyl)-N'-pyrimidin-2-ylmethyl-N-(5,6,7,8-tetrahydro-quinolin-8-yl)-butane-1,4-diamine

HRID 899746Notes

Reaction equation

HRID 899746 reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[N:3][C:2]=1[CH:7]=O.[NH:9]1[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[N:11]=[C:10]1[CH2:18][N:19]([CH:25]1[C:34]2[N:33]=[CH:32][CH:31]=[CH:30][C:29]=2[CH2:28][CH2:27][CH2:26]1)[CH2:20][CH2:21][CH2:22][CH2:23][NH2:24].[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+].[OH-].[Na+]>C1COCC1.Br.CC(O)=O>[NH:9]1[C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=2[N:11]=[C:10]1[CH2:18][N:19]([CH:25]1[C:34]2[N:33]=[CH:32][CH:31]=[CH:30][C:29]=2[CH2:28][CH2:27][CH2:26]1)[CH2:20][CH2:21][CH2:22][CH2:23][NH:24][CH2:7][C:2]1[N:3]=[CH:4][CH:5]=[CH:6][N:1]=1

Participants

7

Reactant 4

HCID 14798Sodium HydroxideHCID 5049666Sodium triacetoxyborohydrideHCID 10126019N'-(1H-benzimidazol-2-ylmethyl)-N'-(5,6,7,8-tetrahydroquinolin-8-yl)butane-1,4-diamineHCID 13751953Pyrimidine-2-carbaldehyde

Product 1

HCID 10127385N-(1H-benzoimidazol-2-ylmethyl)-N'-pyrimidin-2-ylmethyl-N-(5,6,7,8-tetrahydro-quinolin-8-yl)-butane-1,4-diamine

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolventHCID 21893785Acetic Acid Mixture with Hydrobromic AcidSolvent

Procedure

Using General Procedure B: To a solution of the crude aldehyde from above (332 mg) and N′-(1H-benzoimidazol-2-ylmethyl)-N′-(5,6,7,8-tetrahydro-quinolin-8-yl)-butane-1,4-diamine (49 mg, 0.14 mmol) in THF (2 mL) was added NaBH(OAc)3 (89 mg, 0.42 mmol) and the mixture was stirred at room temperature for 1.5 h. The crude material was dissolved in saturated HBr/AcOH (2 mL) and stirred at room temperature for 5 minutes. The solution was made basic with 10 N NaOH(aq) and extracted with CH2Cl2 (3×15 mL). The combined organic extracts were dried (MgSO4) and concentrated in vacuo. Purification of the crude material by column chromatography on silica gel (200:5:1 CH2Cl2/MeOH/NH4OH) afforded a yellow oil (44 mg).

Workup

  1. stirringstirred at room temperature for 5 minutes
  2. extractionextracted with CH2Cl2 (3×15 mL)
  3. dry with materialThe combined organic extracts were dried (MgSO4)
  4. concentrationconcentrated in vacuo
  5. customPurification of the crude material by column chromatography on silica gel (200:5:1 CH2Cl2/MeOH/NH4OH)

Sources & evidence

ORD record
ord-b686d0e23c39411481fbdafea9f52a46
Source dataset
uspto-grants-2008_04
Patent number
US07354934B2

Reaction notes

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