HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → (4R)-1-(5-chloro-3-{5-[2-(dimethylamino)ethyl]-2-methoxyphenyl}-1-{[4-methoxy-2-(trifluoro methoxy)phenyl]sulfonyl}-2-oxo-2,3-dihydro-1H-indol-3-yl)-4-hydroxy-N,N-dimethyl-L-prolin amide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 59867806 | HCID 59867806 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (4R)-1-(5-chloro-3-{5-[2-(dimethylamino)ethyl]-2-methoxyphenyl}-1-{[4-methoxy-2-(trifluoro methoxy)phenyl]sulfonyl}-2-oxo-2,3-dihydro-1H-indol-3-yl)-4-hydroxy-N,N-dimethyl-L-prolin amide | HCID 59867773 | — |
Reaction Steps
A mixed solution of 150 mg of the compound obtained in Example 218, a solution of 2 mol/L dimethylamine in THF (0.22 ml), 63 mg of acetic acid, 95 mg of sodium triacetoxy borohydride, in CHCl3 (1.5 ml) was stirred at room temperature for one hour. A saturated aqueous solution of NaHCO3 was added to the reaction solution, and the resulting mixture was extracted with CHCl3. The extract was dried over Na2SO4, then, the drying agent was separated by filtration and the solvent was evaporated under reduced pressure. Purification was carried out by a preparative TLC plate (1 mm; mobile phase: CHCl3/MeOH=8/1; v/v) to obtain 75 mg of the title compound (colorless solid).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08030499B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-d41da3e3cac54c9b8ebff1fc80a4f658 |
| Source note | uspto-grants-2011_10 |