Triethylamine → HCID 69005605, compound

HRID 2103403Notes

Reaction equation

HRID 2103403 reaction equation
[F:1][C:2]([F:23])([F:22])[C:3]1[CH:8]=[CH:7][N:6]=[C:5]([N:9]2[CH:13]=[C:12]([C:14]([N:16]3[CH2:20][CH2:19][C@H:18]([NH2:21])[CH2:17]3)=[O:15])[N:11]=[CH:10]2)[CH:4]=1.[OH:24][C:25]1([C:32]2[CH:33]=[N:34][C:35]([C:38]3[N:43]=[CH:42][CH:41]=[CH:40][N:39]=3)=[CH:36][CH:37]=2)[CH2:30][CH2:29][C:28](=O)[CH2:27][CH2:26]1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(N(CC)CC)C>C(Cl)Cl.CCOC(C)=O>[N:39]1[CH:40]=[CH:41][CH:42]=[N:43][C:38]=1[C:35]1[N:34]=[CH:33][C:32]([C:25]2([OH:24])[CH2:30][CH2:29][CH:28]([NH:21][C@H:18]3[CH2:19][CH2:20][N:16]([C:14]([C:12]4[N:11]=[CH:10][N:9]([C:5]5[CH:4]=[C:3]([C:2]([F:1])([F:22])[F:23])[CH:8]=[CH:7][N:6]=5)[CH:13]=4)=[O:15])[CH2:17]3)[CH2:27][CH2:26]2)=[CH:37][CH:36]=1

Participants

7

Procedure

To a solution of (3S)-1-({1-[4-(trifluoromethyl)pyridin-2-yl]-1H-imidazol-4-yl}carbonyl)pyrrolidin-3-amine (50 mg, 0.15 mmol) and 4-hydroxy-4-(6-pyrimidin-2-ylpyridin-3-yl)cyclohexanone (41 mg, 0.15 mmol) in methylene chloride (3 mL) was added sodium triacetoxyborohydride (36 mg, 0.17 mmol) followed by triethylamine (0.086 mL, 0.61 mmol). After being stirred at room temperature for 2 h, EtOAc (50 mL) was added. The solution was washed with NaHCO3 solution and water, dried (MgSO4) and concentrated. Purification by HPLC provided two isomers. MS (M+H) 579.3 for both isomers.

Workup

  1. washThe solution was washed with NaHCO3 solution and water
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated
  4. customPurification by HPLC
  5. customprovided two isomers

Sources & evidence

ORD record
ord-3d82eb89aef043c4aac76296f481c7f1
Source dataset
uspto-grants-2009_08
Patent number
US07576089B2

Reaction notes

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