Phenyl glycidyl ether → HCID 71253974, compound

HRID 332106Notes

Reaction equation

HRID 332106 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]1[CH:11]=[N:12][C:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:14][C:5]2=1.[O:20]([CH2:27][CH:28]1[CH2:30][O:29]1)[C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:30][CH:28]([OH:29])[CH2:27][O:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[C:6]1[CH:11]=[N:12][C:13]([C:15]([O:17][CH2:18][CH3:19])=[O:16])=[CH:14][C:5]2=1

Participants

3

Procedure

Following Representative Procedure 1, the title compound ethyl 6-bromo-9-(2-hydroxy-3-phenoxypropyl)-9H-pyrido[3,4-b]indole-3-carboxylate was prepared from ethyl 6-bromo-9H-pyrido[3,4-b]indole-3-carboxylate and phenoxymethyloxirane in 71% yield.

Sources & evidence

ORD record
ord-534fb7b449984f7ea4495751ba143c9c
Source dataset
uspto-grants-2014_11
Patent number
US08877797B2

Reaction notes

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