Water → (E)-3-(6-aminopyridin-3-yl)-N-methyl-N-(3-methylbenzo[b]thiophen-2-ylmethyl)acrylamide

HRID 1921066Notes

Reaction equation

HRID 1921066 reaction equation
[CH3:1][C:2]1[C:3]2[CH:13]=[CH:12][CH:11]=[CH:10][C:4]=2[S:5][C:6]=1[CH2:7][NH:8][CH3:9].[NH2:14][C:15]1[N:20]=[CH:19][C:18](/[CH:21]=[CH:22]/[C:23]([OH:25])=O)=[CH:17][CH:16]=1.C1C=CC2N(O)N=NC=2C=1.O.C1CCC(N=C=NC2CCCCC2)CC1>CN(C=O)C.C(Cl)Cl>[NH2:14][C:15]1[N:20]=[CH:19][C:18](/[CH:21]=[CH:22]/[C:23]([N:8]([CH3:9])[CH2:7][C:6]2[S:5][C:4]3[CH:10]=[CH:11][CH:12]=[CH:13][C:3]=3[C:2]=2[CH3:1])=[O:25])=[CH:17][CH:16]=1

Participants

7

Reactant 5

HCID 962WaterHCID 10868DicyclohexylcarbodiimideHCID 757711-HydroxybenzotriazoleHCID 10487224(2E)-3-(6-aminopyridin-3-yl)prop-2-enoic acidHCID 22593745N-methyl(3-methylbenzo[b]thiophen-2-yl)methanamine

Product 1

HCID 22593722(E)-3-(6-aminopyridin-3-yl)-N-methyl-N-(3-methylbenzo[b]thiophen-2-ylmethyl)acrylamideYield 72.2%

Reagents, catalysts & solvents 1

HCID 22350042dichloromethane N,N-dimethylformamideSolvent

Procedure

To a stirred solution of 3-methyl-2-(methylaminomethyl)benzo[b]thiophene (0.30 g, 1.6 mmole) in 1:1 DMF/CH2Cl2 was added (E)-3-(6-aminopyridin-3-yl)acrylic acid (0.33 g, 2 mmole), HOBt.H2O (0.27 g, 2 mmole), and DCC (0.41 g, 2 mmole). The reaction was stirred for 16 hr, then was concentrated under vacuum. The residue was taken up in CHCl3, washed with H2O, dried (Na2SO4) and concentrated. Purification by flash chromatography on silica gel (4% methanol/CHCl3) gave the title compound (0.39 g, 72%) as a pale yellow solid: LCMS (ES) m/e 338.2 (M+H)+.

Workup

  1. concentrationwas concentrated under vacuum
  2. washwashed with H2O
  3. dry with materialdried (Na2SO4)
  4. concentrationconcentrated
  5. customPurification by flash chromatography on silica gel (4% methanol/CHCl3)

Sources & evidence

ORD record
ord-fdbda2a1a43d4a23b573f7dad33380f5
Source dataset
uspto-grants-2012_05
Patent number
US08173646B2

Reaction notes

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