Triethylamine → HCID 69005605, compound
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]=1Participants
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
- washThe solution was washed with NaHCO3 solution and water
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customPurification by HPLC
- customprovided two isomers
Sources & evidence
- ORD record
- ord-3d82eb89aef043c4aac76296f481c7f1
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576089B2
Reaction notes
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