HCID 45787562, compound → HCID 58207989, compound

HRID 1958506Notes

Reaction equation

HRID 1958506 reaction equation
Br[C:2]1[S:6][C:5]([O:7][CH:8]([CH3:10])C)=[N:4][CH:3]=1.[C:11]1([CH3:29])[CH:16]=[CH:15][CH:14]=[CH:13][C:12]=1[C:17]1[C:18]2[N:19]([CH:26]=[CH:27][N:28]=2)[CH:20]=[C:21](B(O)O)[CH:22]=1>>[CH2:8]([O:7][C:5]1[S:6][C:2]([C:21]2[CH:22]=[C:17]([C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=3[CH3:29])[C:18]3[N:19]([CH:26]=[CH:27][N:28]=3)[CH:20]=2)=[CH:3][N:4]=1)[CH3:10]

Participants

3

Reactant 2

HCID 45787562HCID 45787562, compoundHCID 67008224HCID 67008224, compound

Product 1

HCID 58207989HCID 58207989, compound

Procedure

Example 190 was prepared using the procedure describe for Example 34, step 4 from 5-bromo-2-(isopropyloxy)thiazole and 8-o-tolylimidazo[1,2-a]pyridin-6-ylboronic acid. LCMS (Conditions C): Tr 2.63 min.; (M+H)+: 336.31

Workup

  1. customExample 190 was prepared
  2. customTr 2.63 min.

Sources & evidence

ORD record
ord-9560509728fc4eaf9403681ab82f1de8
Source dataset
uspto-grants-2013_04
Patent number
US08410128B2

Reaction notes

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