HCID 86722850, compound → HCID 178493508, compound

HRID 1778784Notes

Reaction equation

HRID 1778784 reaction equation
[F:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([O:10][CH3:11])=[C:4]([F:12])[C:3]=1[C:13]1[N:18]=[C:17]2[NH:19][N:20]=[C:21](I)[C:16]2=[CH:15][N:14]=1.[OH:23][CH:24]([CH3:45])[CH2:25][N:26]1[CH2:34][C:33]2[C:28](=[CH:29][CH:30]=[C:31](B3OC(C)(C)C(C)(C)O3)[CH:32]=2)[C:27]1=[O:44]>>[F:1][C:2]1[C:7]([O:8][CH3:9])=[CH:6][C:5]([O:10][CH3:11])=[C:4]([F:12])[C:3]=1[C:13]1[N:18]=[C:17]2[NH:19][N:20]=[C:21]([C:31]3[CH:32]=[C:33]4[C:28](=[CH:29][CH:30]=3)[C:27](=[O:44])[N:26]([CH2:25][CH:24]([OH:23])[CH3:45])[CH2:34]4)[C:16]2=[CH:15][N:14]=1

Participants

3

Reactant 2

HCID 86722850HCID 86722850, compoundHCID 178493522HCID 178493522, compound

Product 1

HCID 178493508HCID 178493508, compound

Procedure

This compound was prepared by using procedures analogous to those described for the synthesis of Example 4, Step 2 starting from 6-(2,6-difluoro-3,5-dimethoxyphenyl)-3-iodo-1H-pyrazolo[3,4-d]pyrimidine and 2-(2-hydroxypropyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoindolin-1-one. LCMS (M+H)+=482.1.

Workup

  1. customThis compound was prepared

Sources & evidence

ORD record
ord-7586cd752e8f42f2b7282e4670d56a44
Source dataset
uspto-grants-2016_02
Patent number
US09266892B2

Reaction notes

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