4-Fluorobenzyl bromide → N-Ethylcarbamate 5-(4-fluorobenzyloxy)-8-methyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrrole

HRID 546321Notes

Reaction equation

HRID 546321 reaction equation
[CH2:1]([NH:3][C:4](=[O:6])[O-:5])[CH3:2].[OH:7][C:8]1[CH:9]=[CH:10][C:11]2[CH:12]([CH3:20])[CH:13]3[CH2:17][NH:16][CH2:15][CH:14]3[C:18]=2[CH:19]=1.[F:21][C:22]1[CH:29]=[CH:28][C:25]([CH2:26]Br)=[CH:24][CH:23]=1>>[CH2:1]([NH:3][C:4](=[O:5])[O-:6])[CH3:2].[F:21][C:22]1[CH:29]=[CH:28][C:25]([CH2:26][O:7][C:8]2[CH:9]=[CH:10][C:11]3[CH:12]([CH3:20])[CH:13]4[CH2:17][NH:16][CH2:15][CH:14]4[C:18]=3[CH:19]=2)=[CH:24][CH:23]=1

Participants

3

Reactant 2

HCID 680214-Fluorobenzyl bromideHCID 86602864N-Ethylcarbamate 5-hydroxy-8-methyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrrole

Product 1

HCID 86602870N-Ethylcarbamate 5-(4-fluorobenzyloxy)-8-methyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrrole

Procedure

The subtitle compound was prepared by the method of Example 43, Step B utilizing N-ethylcarbamate-5-hydroxy-8-methyl-1,2,3,3a,8,8a-hexahydroindeno[1,2-c]pyrrole (from Example 43, Step A) (0.1 mmol) and 4-fluorobenzyl bromide. The crude product was obtained without further purification. MS calculated for C22H24FNO3+H: 370, observed: 370.

Sources & evidence

ORD record
ord-930896a960044dffadcd75f061f98e4d
Source dataset
uspto-grants-2011_05
Patent number
US07935830B2

Reaction notes

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