Methyl 4-Formylbenzoate → HCID 68292076, compound
Reaction equation
Cl.Cl.[O:3]1[C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=2[O:6][CH2:5][C@@H:4]1[C:13]1[CH:25]=[CH:24][C:16]([CH2:17][N:18]2[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]2)=[CH:15][CH:14]=1.[CH3:26][O:27][C:28](=[O:37])[C:29]1[CH:34]=[CH:33][C:32]([CH:35]=O)=[CH:31][CH:30]=1.C([BH3-])#N.[Na+].CCN(C(C)C)C(C)C>CO.C(O)(=O)C>[CH3:26][O:27][C:28](=[O:37])[C:29]1[CH:34]=[CH:33][C:32]([CH2:35][N:21]2[CH2:20][CH2:19][N:18]([CH2:17][C:16]3[CH:15]=[CH:14][C:13]([C@@H:4]4[O:3][C:8]5[CH:9]=[CH:10][CH:11]=[CH:12][C:7]=5[O:6][CH2:5]4)=[CH:25][CH:24]=3)[CH2:23][CH2:22]2)=[CH:31][CH:30]=1Participants
7
Procedure
A solution of 1-[(S)-4-(2,3-dihydro-benzo[1,4]dioxin-2-yl)-benzyl]-piperazine dihydrochloride (80 mg, 0.21 mmol), 4-formyl-benzoic acid methyl ester (41 mg, 0.25 mmol), sodium cyanoborohydride (26 mg, 0.42 mmol), and DIPEA (0.07 mL, 0.42 mmol) in MeOH (5 mL) is treated with 2 drops of acetic acid. The resulting mixture is stirred at room temperature for 16 h, concentrated, diluted with water, and extracted with ethyl acetate. The organic layer is washed with brine, dried over Na2SO4, filtered, and concentrated. The residue is purified by flash chromatography eluting with a gradient of 0-10% MeOH in DCM to give 4-{4-[(S)-4-(2,3-dihydro-benzo[1,4]dioxin-2-yl)-benzyl]-piperazin-1-ylmethyl}-benzoic acid methyl ester.
Workup
- concentrationconcentrated
- additiondiluted with water
- extractionextracted with ethyl acetate
- washThe organic layer is washed with brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated
- customThe residue is purified by flash chromatography
- washeluting with a gradient of 0-10% MeOH in DCM
Sources & evidence
- ORD record
- ord-aaf934ea6ef0474eb3075650aaecea62
- Source dataset
- uspto-grants-2015_02
- Patent number
- US08946203B2
Reaction notes
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