HCID 57562622, compound → Diisopropylethylamine

HRID 1725470Notes

Reaction equation

HRID 1725470 reaction equation
Cl[CH2:2][C:3]1[N:8]=[C:7](NC2SC=CN=2)[CH:6]=C[CH:4]=1.Cl[C:16]1[C:17](F)=C(C=C[CH:29]=1)C(N1CCNCC1)=O>CN(C)C=O>[CH:16]([N:8]([CH2:7][CH3:6])[CH:3]([CH3:2])[CH3:4])([CH3:17])[CH3:29]

Participants

4

Procedure

A mixture of 2.70 g of 6-(chloromethyl)-N-thiazol-2-ylpyridin-2-amine, 4.00 g of 1-(3-chloro-2-fluorobenzoyl)piperazine obtained in Reference Example 1, 6.25 ml of N,N-diisopropylethylamine and 30 ml of dimethylformamide was stirred at 90° C. for 2 hours. The reaction solution was diluted with ethyl acetate and then washed with water and brine. The resulting organic layer was dried over magnesium sulfate and filtered, and the filtrate was concentrated. The resulting residue was purified by a silica gel column chromatography (eluent: chloroform to chloroform/methanol=10/1). Then, the obtained compound was suspended in ethyl acetate, and filtered and collected to give the title compound as a colorless amorphous substance.

Sources & evidence

ORD record
ord-b21677e808ab4ddb9afda0c22f864cf7
Source dataset
uspto-grants-2009_02
Patent number
US07491720B2

Reaction notes

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