Potassium Carbonate → HCID 70217236, compound

HRID 1779636Notes

Reaction equation

HRID 1779636 reaction equation
[O:1]1[CH2:3][C@H:2]1[CH2:4][O:5][C:6]1[CH:14]=[CH:13][CH:12]=[C:11]2[C:7]=1[CH:8]=[CH:9][NH:10]2.[Cl:15][C:16]1[CH:30]=[CH:29][C:19]2[S:20][CH:21]=[C:22]([C:23]3[CH2:24][CH2:25][NH:26][CH2:27][CH:28]=3)[C:18]=2[CH:17]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C>[Cl:15][C:16]1[CH:30]=[CH:29][C:19]2[S:20][CH:21]=[C:22]([C:23]3[CH2:24][CH2:25][N:26]([CH2:3][C@H:2]([OH:1])[CH2:4][O:5][C:6]4[CH:14]=[CH:13][CH:12]=[C:11]5[C:7]=4[CH:8]=[CH:9][NH:10]5)[CH2:27][CH:28]=3)[C:18]=2[CH:17]=1

Participants

5

Reactant 3

HCID 11430Potassium CarbonateHCID 10943254(2s)-Glycidyl indol-4-yl etherHCID 18797366HCID 18797366, compound

Product 1

HCID 70217236HCID 70217236, compound

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

The title compound was prepared in a fashion similar to that described in Example 1 using (S)-(+)-4-(oxiranylmethoxy)-1H-indole (0.053 g, 0.028 mmol) and the hydrochloride salt of 5-chloro-3-(1,2,3,6-tetrahydropyridin-4-yl)benzo[b]thiophene (0.081 g, 0.028 mmol) using ethanol as reaction solvent and 1.1 equivalents of potassium carbonate (0.043 g, 0.031 mmol). Yield 0.103 g (83%) of a tan foam. mp 93°-97° C. FDMS m/e=438 (M+ of free base). α[D]589 =+7.5 (c=1.06, dimethylsufoxide)

Sources & evidence

ORD record
ord-688344e703124aaabe6f50fe24f1488f
Source dataset
uspto-grants-1997_05
Patent number
US05627196

Reaction notes

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