1H-Pyrrolo(2,3-b)pyridine → 4,4-Di-(7-azaindol-3-yl)-1-butanol

HRID 6939

Reaction equation

HRID 6939 reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][N:8]=2)[CH:3]=[CH:2]1.C[O:11][CH:12]1[CH2:16][CH2:15][CH2:14]O1>>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][N:8]=2)[C:3]([CH:14]([C:3]2[C:4]3[C:9](=[N:8][CH:7]=[CH:6][CH:5]=3)[NH:1][CH:2]=2)[CH2:15][CH2:16][CH2:12][OH:11])=[CH:2]1

Participants

3

Reactant 2

HCID 92221H-Pyrrolo(2,3-b)pyridineHCID 47519Tetrahydro-2-methoxyfuran

Product 1

HCID 98361644,4-Di-(7-azaindol-3-yl)-1-butanol

Procedure

This compound is prepared in the same way as described in example 1/1 starting from 7-azaindol and 2-methoxy-tetrahydrofuran.

Workup

  1. customThis compound is prepared in the same way

Sources & evidence

ORD record
ord-eede2b3d64ad403cbc6219dd7b894bcc
Source dataset
uspto-grants-2006_08
Patent number
US07084166B2

Linked notes

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