Acetic Acid → HCID 11291125, compound
Reaction equation
O=[C:2]1[CH2:7][CH2:6][CH:5]([O:8][C:9]2[CH:17]=[CH:16][C:12]([C:13]([NH2:15])=[O:14])=[CH:11][CH:10]=2)[CH2:4][CH2:3]1.[C:18]1([CH2:24][CH2:25][CH2:26][NH2:27])[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.C(O)(=O)C>C(Cl)Cl>[C:18]1([CH2:24][CH2:25][CH2:26][NH:27][CH:2]2[CH2:7][CH2:6][CH:5]([O:8][C:9]3[CH:17]=[CH:16][C:12]([C:13]([NH2:15])=[O:14])=[CH:11][CH:10]=3)[CH2:4][CH2:3]2)[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Combine 4-(4-oxo-cyclohexyloxy)-benzamide (20 mg, 0.085 mmol), 3-phenyl-propylamine (11 mg, 0.085 mmol), triacetoxyborohydride (23 mg, 0.111 mmol) and acetic acid (5 μL, 0.085 mmol) in CH2Cl2 (1 mL). Let stir overnight. Purify by SCX column (ammonia in methanol 2.0M). Triturate the residue with EtOAc/hexanes 1/1 to provide a white powder (25 mg, 86%).
Workup
- customPurify by SCX column (ammonia in methanol 2.0M)
- customTriturate the residue with EtOAc/hexanes 1/1
Sources & evidence
- ORD record
- ord-30ff7548533a413cb2f3d05e86970c8a
- Source dataset
- uspto-grants-2007_03
- Patent number
- US07196100B2
Reaction notes
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