1-(Benzenesulfonyl)-3-iodo-1H-pyrrolo[2,3-b]pyridine → HCID 57619206, compound

HRID 1367410Notes

Reaction equation

HRID 1367410 reaction equation
[C:1]1([S:7]([N:10]2[C:14]3=[N:15][CH:16]=[C:17](Cl)[CH:18]=[C:13]3[C:12](I)=[CH:11]2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C1(S([N:30]2[C:34]3=[N:35][CH:36]=[CH:37][CH:38]=C3C(I)=[CH:31]2)(=O)=O)C=CC=CC=1>>[C:1]1([S:7]([N:10]2[C:14]3=[N:15][CH:16]=[CH:17][CH:18]=[C:13]3[C:12]([CH2:38][C:37]3[CH:36]=[N:35][C:34]([S:7]([CH3:1])(=[O:9])=[O:8])=[N:30][CH:31]=3)=[CH:11]2)(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

3

Reactant 2

HCID 242292281-(Benzenesulfonyl)-3-iodo-1H-pyrrolo[2,3-b]pyridineHCID 242292391-Benzenesulfonyl-5-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine

Product 1

HCID 57619206HCID 57619206, compound

Procedure

was prepared following the protocol of Scheme 191, substituting 1 benzenesulfonyl-5-chloro-3-iodo-1H-pyrrolo[2,3-b]pyridine 581 with 1-benzenesulfonyl-3-iodo-1H-pyrrolo[2,3-b]pyridine in Step 1.

Workup

  1. customwas prepared

Sources & evidence

ORD record
ord-6db9f4611285456dba8cc305eb0ee8e9
Source dataset
uspto-grants-2011_02
Patent number
US07893075B2

Reaction notes

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