Hydrochloric Acid → HCID 19599900, compound
Reaction equation
C(O[C:6]([N:8]([CH2:10][C:11]1[O:32][C:14]2[CH2:15][N:16]([C:19](=[O:31])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[CH2:17][CH2:18][C:13]=2[CH:12]=1)C)=O)(C)(C)C.[ClH:33]>CO>[ClH:33].[CH3:6][NH:8][CH2:10][C:11]1[O:32][C:14]2[CH2:15][N:16]([C:19](=[O:31])[CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][C:25]3[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=3)[CH2:17][CH2:18][C:13]=2[CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
1-[2-(N-tert-Butoxycarbonyl-N-methylaminomethyl)-5,7-dihydro-4H-furo[2,3-c]pyridin-6-yl]-6-phenylhexan-1-one 0.191 g was dissolved in 2 ml of methanol; 0.5 ml of concentrated hydrochloric acid was added, followed by stirring for 30 minutes. This mixture was concentrated to yield the desired product.
Workup
- concentrationThis mixture was concentrated
Sources & evidence
- ORD record
- ord-8cb15a09df9542f4ae2d5b819f351965
- Source dataset
- uspto-grants-1999_12
- Patent number
- US05998433
Reaction notes
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