Morpholine → 3-(4-Morpholinylmethyl)-7-(4-phenyl-1-piperidinyl)-1,2,4-triazolo[4,3-a]pyridine-8-carbonitrile

HRID 587656Notes

Reaction equation

HRID 587656 reaction equation
[C:1]([C:3]1[C:4]2[N:5]([C:21]([CH:24]=O)=[N:22][N:23]=2)[CH:6]=[CH:7][C:8]=1[N:9]1[CH2:14][CH2:13][CH:12]([C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:11][CH2:10]1)#[N:2].[NH:26]1[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+]>C(Cl)Cl>[N:26]1([CH2:24][C:21]2[N:5]3[CH:6]=[CH:7][C:8]([N:9]4[CH2:14][CH2:13][CH:12]([C:15]5[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=5)[CH2:11][CH2:10]4)=[C:3]([C:1]#[N:2])[C:4]3=[N:23][N:22]=2)[CH2:31][CH2:30][O:29][CH2:28][CH2:27]1

Participants

5

Procedure

To a solution of D9 (0.065 g, 0.196 mmol) in DCM (2.5 ml) were added morpholine (0.026 g, 0.294 mmol) and sodium triacetoxy-borohydride (0.062 mg, 0.294 mmol). The resulting mixture was stirred at r.t. for 1 day. The reaction mixture was washed with H2O, dried (MgSO4) and concentrated in vacuo. The crude product thus obtained was purified by column chromatography (silica gel; DCM/MeOH up to 3% as eluent). The desired fractions were collected and concentrated in vacuo to yield final compound E11 (0.04 g, 51%) as a white solid.

Workup

  1. washThe reaction mixture was washed with H2O
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated in vacuo
  4. customThe crude product thus obtained
  5. customwas purified by column chromatography (silica gel; DCM/MeOH up to 3% as eluent)
  6. customThe desired fractions were collected
  7. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-77e2ad3d256140a0bf14794e02887e51
Source dataset
uspto-grants-2016_01
Patent number
US09226930B2

Reaction notes

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