Hydrogen Bromide → HCID 178419865, compound
Reaction equation
C(OC([N:11]1[CH:23]([C:24]2[NH:28][N:27]=[N:26][N:25]=2)[CH2:22][C:21]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[NH:14][C:13]=2[CH2:12]1)=O)C1C=CC=CC=1.Br.CCOCC>C(O)(=O)C>[NH:28]1[C:24]([CH:23]2[CH2:22][C:21]3[C:20]4[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=4)[NH:14][C:13]=3[CH2:12][NH:11]2)=[N:25][N:26]=[N:27]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
(3RS)-2-Benzyloxycarbonyl-3-(1H-tetrazol-5-yl)-1,2,3,4-tetrahydro-β-carboline (0.3 g) is dissolved in acetic acid (1 ml) and thereto is added dropwise a 25% solution of HBr in acetic acid (2 ml). The mixture is stirred at room temperature for 20 minutes, and thereto is added ether. The precipitates are collected by filtration, washed with ether and dried to give the title compound (0.257 g, quantitatively) as pale yellow powder.
Workup
- filtrationThe precipitates are collected by filtration
- washwashed with ether
- customdried
Sources & evidence
- ORD record
- ord-f7a18b5a605743848048fd6678ac96d5
- Source dataset
- uspto-grants-1986_12
- Patent number
- US04628057
Reaction notes
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