Lithium Hydroxide → HCID 15887619, compound

HRID 377106Notes

Reaction equation

HRID 377106 reaction equation
[Cl:1][C:2]1[CH:27]=[CH:26][C:5]([O:6][C:7]2[N:12]=[CH:11][C:10]([NH:13][C:14]([C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[O:22]C(=O)C)=[O:15])=[CH:9][CH:8]=2)=[C:4]([CH3:28])[CH:3]=1.[OH-].[Li+]>O1CCCC1>[Cl:1][C:2]1[CH:27]=[CH:26][C:5]([O:6][C:7]2[N:12]=[CH:11][C:10]([NH:13][C:14](=[O:15])[C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[OH:22])=[CH:9][CH:8]=2)=[C:4]([CH3:28])[CH:3]=1

Participants

4

Conditions

Temperature
22 °C

Procedure

Acetic acid 2-(6-(4-chloro-2-methyl-phenoxy)-pyridin-3-ylcarbamoyl)-phenyl ester (304 mg, 0.77 mmol) dissolved in tetrahydrofuran (3.8 mL) was treated with an aqueous lithium hydroxide solution (1.0 M, 3.8 mL, 3.8 mmol). The solution was stirred for 30 minutes at 22° C. then quenched with aqueous saturated NH4Cl. The mixture was diluted with ethyl acetate then the organics were washed with water, 2× saturated NaHCO3, saturated NaCl, dried over Na2SO4 and concentrated in vacuo. MS (m/z): 354/356 (M+H)+ ; C19H15N2O3Cl requires 354.8.

Workup

  1. customthen quenched with aqueous saturated NH4Cl
  2. additionThe mixture was diluted with ethyl acetate
  3. washthe organics were washed with water, 2× saturated NaHCO3, saturated NaCl
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-93ddaa9b43704fe2a182ab3584aaf88a
Source dataset
uspto-grants-2000_02
Patent number
US06022884

Reaction notes

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