HCID 943226, compound → HCID 70511232, compound
Reaction equation
C(OC([N:8]1[CH2:23][CH2:22][CH2:21][C@H:9]1[C:10]([NH:12][CH2:13][CH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1)=[O:11])=O)(C)(C)C.C(OCC)(=O)C.[ClH:30]>CCOCC>[ClH:30].[C:15]1([CH2:14][CH2:13][NH:12][C:10](=[O:11])[C@@H:9]2[CH2:21][CH2:22][CH2:23][NH:8]2)[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 1-(tert-butyloxycarbonyl)-N-(2-phenylethyl)-L-prolinamide (2.46 g.) in ethyl acetate-hydrogen chloride (3.9 N, 30 ml.) was stirred for 20 minutes at room temperature, then diluted with ether (to about 200 ml.). The solvents were decanted from the resulting gum, which was triturated with ether, affording crystalline N-(2-phenylethyl)-L-prolinamide hydrochloride (1.91 g., m.r. 147°-150° ).
Workup
- customThe solvents were decanted from the resulting gum, which
- customwas triturated with ether
Sources & evidence
- ORD record
- ord-a2711669812d498bbaf9f47f16d2e2f7
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04450155
Reaction notes
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