Hydrochloric Acid → HCID 68577659, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]([N:17]2[CH2:21][CH2:20][CH2:19][C@H:18]2[CH2:22][N:23]2[CH2:27][CH2:26][CH2:25][CH2:24]2)=[O:16])=[CH:11][CH:10]=1.[ClH:28]>C(OCC)C.CO>[ClH:28].[ClH:28].[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][O:8][C:9]1[CH:10]=[CH:11][C:12]([C:15]([N:17]2[CH2:21][CH2:20][CH2:19][C@H:18]2[CH2:22][N:23]2[CH2:24][CH2:25][CH2:26][CH2:27]2)=[O:16])=[CH:13][CH:14]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of [4-(Pyridin-2-ylmethoxy)-phenyl]-(2-(S)-pyrrolidin-1-ylmethyl-pyrrolidin-1-yl)-methanone (1.94 g, 5.3 mmol) in diethyl ether and methanol is added a solution of HCl in ether (10.7 mmol, 1M). The mixture is concentrated, and the oily residue is dissolved in a mixture of diethyl ether and methanol and again concentrated. The solid is triturated with petroleum ether, and the solid is dried to yield 2.2 g of a yellowish solid MS (ES+) 1366.3
Workup
- concentrationThe mixture is concentrated
- dissolutionthe oily residue is dissolved in a mixture of diethyl ether and methanol
- concentrationagain concentrated
- customThe solid is triturated with petroleum ether
- customthe solid is dried
Sources & evidence
- ORD record
- ord-54c7643fdf42407fa1ea3749d1a5a762
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696234B2
Reaction notes
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