Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)- → HCID 10268868, compound

HRID 1796085Notes

Reaction equation

HRID 1796085 reaction equation
Br[C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=2)[CH:5]=[CH:4][CH:3]=1.C([Sn](CCCC)(CCCC)[C:19]1[N:23]2[CH:24]=[CH:25][C:26]([C:28]([F:31])([F:30])[F:29])=[N:27][C:22]2=[N:21][CH:20]=1)CCC>>[F:30][C:28]([F:29])([F:31])[C:26]1[CH:25]=[CH:24][N:23]2[C:19]([C:2]3[N:7]=[C:6]([C:8]4[CH:13]=[CH:12][CH:11]=[CH:10][N:9]=4)[CH:5]=[CH:4][CH:3]=3)=[CH:20][N:21]=[C:22]2[N:27]=1

Participants

3

Reactant 2

HCID 11294484Imidazo[1,2-a]pyrimidine, 3-(tributylstannyl)-7-(trifluoromethyl)-HCID 117911522-Bromo-6-(pyridin-2-yl)pyridine

Product 1

HCID 10268868HCID 10268868, compoundYield 33.7%

Procedure

6-Bromo-2,2′-bipyridine (0.35 g, 1.44 mmol) was coupled to 3-tributylstannyl-7-trifluoromethylimidazo[1,2-α]pyrimidine (1.13 mmol) by the method of Example 1. Purification by chromatography on silica gel eluting with isohexane on a gradient of ethyl acetate (20-100%) and trituration with isohexane gave 6-(7-trifluoromethylimidazo[1,2-α]pyrimidin-3-yl)-2,2′-bipyridine (130 mg) as a pale yellow solid: δH (400 MHz, CDCl3) 7.39-7.43 (2H, m), 7.85 (1H, d, J 8), 7.89-7.94 (1H, m), 7.99 (1H, dd, J 8 and 8), 8.31 (1H, d, J 8), 8.38 (1H, d, J 8), 8.56 (1H, s), 8.75-8.80 (1H, m), 10.53 (1H, d, J 7); m/z (ES+) 342 (M++H).

Workup

  1. customPurification by chromatography on silica gel eluting with isohexane on a gradient of ethyl acetate (20-100%) and trituration with isohexane

Sources & evidence

ORD record
ord-24f52cfe56a048bbb598b80e6ab9ac4f
Source dataset
uspto-grants-2006_04
Patent number
US07030128B2

Reaction notes

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