4-Pentynoic acid → 5-(But-3-ynyl)-3-(2-methoxyphenyl)-1,2,4-oxadiazole

HRID 334558Notes

Reaction equation

HRID 334558 reaction equation
[OH:1][N:2]=[C:3]([NH2:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[O:10][CH3:11].[C:13](O)(=O)[CH2:14][CH2:15][C:16]#[CH:17].C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.Cl>O1CCOCC1>[CH2:16]([C:17]1[O:1][N:2]=[C:3]([C:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=2[O:10][CH3:11])[N:12]=1)[CH2:15][C:14]#[CH:13]

Participants

6

Reactant 4

HCID 224644-Pentynoic acidHCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 4652214N-Hydroxy-2-methoxy-benzamidine

Product 1

HCID 860867965-(But-3-ynyl)-3-(2-methoxyphenyl)-1,2,4-oxadiazoleYield 36.4%

Reagents, catalysts & solvents 1

HCID 312751,4-DioxaneSolvent

Conditions

Temperature
80 °C

Procedure

In a reactor tube, a mixture of N′-hydroxy-2-methoxybenzamidine (598 mg, 3.6 mmol), 4-pentynoic acid (350 mg, 3.6 mmol), HOBT (0.55 g, 3.6 mmol) and EDCI.HCl (1.03 g, 5.4 mmol) in dioxane (7.4 mL) was stirred at R.T for 3 h. After this time the mixture was heated at 80° C. overnight in a reaction block. The mixture was concentrated and the crude product was purified by flash chromatography (Prepacked column 25 g with DCM as eluent) to afford 299 mg of 5-(but-3-ynyl)-3-(2-methoxyphenyl)-1,2,4-oxadiazole (36%) as yellow oil.

Workup

  1. concentrationThe mixture was concentrated
  2. customthe crude product was purified by flash chromatography (Prepacked column 25 g with DCM as eluent)

Sources & evidence

ORD record
ord-cc844894055844f185013e45b45fb86a
Source dataset
uspto-grants-2014_11
Patent number
US08883826B2

Reaction notes

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