Sodium cyanoborohydride → HCID 19029357, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]([CH2:22][CH:23]=O)[CH2:10][C:11]([N:13]2[C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH:15]=[CH:14]2)=[O:12])[CH:5]=[CH:6][C:7]=1[Cl:8].Cl.[C:26]1([C:32]2([OH:38])[CH2:37][CH2:36][NH:35][CH2:34][CH2:33]2)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1.[BH3-]C#N.[Na+]>CO.C1COCC1>[Cl:1][C:2]1[CH:3]=[C:4]([CH:9]([CH2:22][CH2:23][N:35]2[CH2:36][CH2:37][C:32]([OH:38])([C:26]3[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=3)[CH2:33][CH2:34]2)[CH2:10][C:11]([N:13]2[C:17]3[C:16](=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:15]=[CH:14]2)=[O:12])[CH:5]=[CH:6][C:7]=1[Cl:8]Participants
5
Procedure
1-[3-(3,4-dichlorophenyl)-1,5-dioxopentyl]-1H-indole (740 mg), in MeOH/THF (1:1, 30 mL) was treated sequentially with molecular sieves 3A (880 mg), 4-phenyl-4-hydroxypiperidine HCl (880 mg) and NaBH3CN (130 mg). The resulting mixture was stirred at room temperature for 18 hours. The reaction mixture was with quenched with water (20 mL) and diluted with CH2Cl2 (50 mL). The organic layer was separated and the aqueous layer extracted with CH2Cl2 (3×50 mL) The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure to give the crude oil. Silica gel chromatography eluting with 1-2% MeOH/CH2Cl2 gave the title compound (600 mg). Mass spectrum (CI): 521.
Workup
- customwith quenched with water (20 mL)
- additiondiluted with CH2Cl2 (50 mL)
- customThe organic layer was separated
- extractionthe aqueous layer extracted with CH2Cl2 (3×50 mL) The combined organic layers
- dry with materialwere dried over MgSO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customto give the crude oil
- washSilica gel chromatography eluting with 1-2% MeOH/CH2Cl2
Sources & evidence
- ORD record
- ord-10768a809b674a11b60d483621b94105
- Source dataset
- uspto-grants-1997_08
- Patent number
- US05654316
Reaction notes
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