p-Toluenesulfonic acid monohydrate → HCID 57920050, compound

HRID 19338Notes

Reaction equation

HRID 19338 reaction equation
[Cl:1][C:2]1[CH:35]=[CH:34][CH:33]=[CH:32][C:3]=1[O:4][C:5]1[CH2:9][N:8]([C@@H:10]([CH2:27][CH2:28][S:29][CH3:30])[C:11]([NH:13][C:14]2[CH:18]=[CH:17][N:16]([CH2:19][C@@H:20]3[CH2:24][O:23]C(C)(C)[O:21]3)[N:15]=2)=[O:12])[C:7](=[O:31])[CH:6]=1.O.C1(C)C=CC(S(O)(=O)=O)=CC=1>CO>[Cl:1][C:2]1[CH:35]=[CH:34][CH:33]=[CH:32][C:3]=1[O:4][C:5]1[CH2:9][N:8]([C@@H:10]([CH2:27][CH2:28][S:29][CH3:30])[C:11]([NH:13][C:14]2[CH:18]=[CH:17][N:16]([CH2:19][C@@H:20]([OH:21])[CH2:24][OH:23])[N:15]=2)=[O:12])[C:7](=[O:31])[CH:6]=1

Participants

4

Reactant 2

HCID 521998p-Toluenesulfonic acid monohydrateHCID 66899622HCID 66899622, compound

Product 1

HCID 57920050HCID 57920050, compoundYield 74%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
25 °C

Procedure

In a round bottom flask was placed (S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-((R)-2,2-dimethyl-[1,3]dioxolan-4-yl-methyl)-1H-pyrazol-3-yl]-4-methylsulfanyl-butyramide (118 mg, 0.23 mmol), methanol (5 mL) and p-toluenesulfonic acid monohydrate (9 mg). The mixture was stirred at 25° C. for 16 h and then concentrated in vacuo, dissolved in ethyl acetate with a little methanol to solubilize the material and concentrated in vacuo with silica gel (1 g). Purification by Biotage flash chromatography (AnaLogix, 12 g column, 100% ethyl acetate to 10% methanol/ethyl acetate) afforded (S)-2-[4-(2-chloro-phenoxy)-2-oxo-2,5-dihydro-pyrrol-1-yl]-N-[1-((R)-2,3-dihydroxy-propyl)-1H-pyrazol-3-yl]-4-methylsulfanyl-butyramide (80 mg, 74%) as a white foam: HR-ES-MS m/z calculated for C21H25N4O5ClS [M+H]+ 481.1307, observed 491.1307; 1H NMR (300 MHz, DMSO-d6) δ ppm 1.96-2.19 (m, 2H), 2.09 (s, 3H), 2.29-2.48 (m, 2H), 3.21-3.33 (m, 2H), 3.69-3.81 (m, 1H), 3.86 (dd, J=13.5, 7.5 Hz, 1H), 4.09 (dd, J=13.5, 3.8 Hz, 1H), 4.27 (d, J=18.2 Hz, 1H), 4.56 (d, J=18.2 Hz, 1H), 4.71 (t, J=5.6 Hz, 1H), 4.78-4.86 (m, 1H), 4.81 (s, 1H), 4.94 (d, J=5.4 Hz, 1H), 6.41 (d, J=2.1 Hz, 1H), 7.37 (td, J=7.8, 1.8 Hz, 1H), 7.47 (td, J=7.8, 1.4 Hz, 1H), 7.50-7.55 (m, 2H), 7.66 (dd, J=7.8, 1.4 Hz, 1H), 10.72 (s, 1H).

Workup

  1. customIn a round bottom flask was placed
  2. concentrationconcentrated in vacuo
  3. dissolutiondissolved in ethyl acetate with a little methanol
  4. concentrationconcentrated in vacuo with silica gel (1 g)
  5. customPurification by Biotage flash chromatography (AnaLogix, 12 g column, 100% ethyl acetate to 10% methanol/ethyl acetate)

Sources & evidence

ORD record
ord-a203c8fa5c4b4480849bd0f72bc6122f
Source dataset
uspto-grants-2010_06
Patent number
US07741327B2

Reaction notes

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