Calcium Chloride → HCID 87957780, compound
Reaction equation
[Br-:1].[F:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][CH:10]2[CH2:15][CH2:14][N+:13]3([CH2:23][C:22]4[C:17](=[CH:18][CH:19]=[CH:20][C:21]=4[N+:24]([O-])=O)[CH2:16]3)[CH2:12][CH2:11]2)=[CH:5][CH:4]=1.[Cl-].[Ca+2].[Cl-]>[Zn].C(O)C.O>[Br-:1].[NH2:24][C:21]1[CH:20]=[CH:19][CH:18]=[C:17]2[C:22]=1[CH2:23][N+:13]1([CH2:16]2)[CH2:12][CH2:11][CH:10]([CH2:9][C:6]2[CH:7]=[CH:8][C:3]([F:2])=[CH:4][CH:5]=2)[CH2:15][CH2:14]1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
1,3-Dihydro-4′-[4-fluorophenylmethyl]-4-nitro-spiro[2H-isoindole-2,1′-piperidinium] bromide (1.03 g, 2.46 mmol, 1.0 eq), zinc (5.32 g, 81.5 mmol, 33.0 eq), and calcium chloride (0.18 g, 1.60 mmol, 0.65 eq) were refluxed under N2 in 25 ml of a 78% ethanol/water solution. The reaction was worked up after 5 hours by filtering through Celite® and rinsing the cake with methanol. The filtrate was concentrated in vacuo to a mixture of water and an amber oil. The mixture was dissolved in 50 ml of 2-propanol, and concentrated in vacuo to remove excess water. The resulting yellow foam was dissolved in methanol and applied to a 3.5 cm×5 cm quartz column via silica plug. The product was eluted with 20% MeOH/CHCl3 to yield 0.81 g of a yellow foam. NMR (300 MHz, DMSO) δ7.27-7.05 (m, 5H), 6.61-6.53 (m, 2H), 5.43-5.41 (m, 2H), 4.80 (bs, 1H), 4.74 (bs, 2H), 4.63 (bs, 1H), 3.62-3.43 (m, 4H), 2.60 (bd, 2H, J=7 Hz), 1.98-1.59 (m, 5H).
Workup
- filtrationby filtering through Celite®
- washrinsing the cake with methanol
- concentrationThe filtrate was concentrated in vacuo to a mixture of water
- dissolutionThe mixture was dissolved in 50 ml of 2-propanol
- concentrationconcentrated in vacuo
- customto remove excess water
- dissolutionThe resulting yellow foam was dissolved in methanol
- washThe product was eluted with 20% MeOH/CHCl3
Sources & evidence
- ORD record
- ord-08b637a9b2ef40f29aeb47cd4aa8a33d
- Source dataset
- uspto-grants-2002_12
- Patent number
- US06492400B1
Reaction notes
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