Benzoyl chloride → HCID 10998603, compound

HRID 1785594Notes

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:10](Cl)(=[O:17])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.COC1C=C(C=CC=1)C(Cl)=O>>[C:10]([C:3]1[C:4]2[C:9](=[N:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1)(=[O:17])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1

Participants

Reactant 3

HCID 7412Benzoyl chloride

HCID 92221H-Pyrrolo(2,3-b)pyridine

HCID 74374m-Anisoyl chloride

Product 1

HCID 10998603HCID 10998603, compound

Procedure

Compound 41 was prepared from 7-azaindole 2 using aluminum chloride as described previously for the synthesis of Compound 25, with benzoyl chloride substituted for m-methoxy-benzoyl chloride.

Sources & evidence

ORD record: ord-395b2e6f341c4c33875dea5e7301a11f
Source dataset: uspto-grants-2009_03
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07504509B2

Reaction notes

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