Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 66985947 | HCID 66985947 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66769308 | HCID 66769308 | — |
Reaction Steps
1.29 g methyl 5-tert-butyl-2-methoxy-3-({1-methyl-7-[4-(1-methyl-pyrrolidine-2-carbonyl)-piperazin-1-ylmethyl]-1H-indole-2-carbonyl}-amino)-benzoate are dissolved in 25 ml of tetrahydrofuran, combined with 4 ml of 4 N sodium hydroxide solution and heated for 2 hours to 40° C. Then the mixture is heated for 12 hours to 60° C., then a further 2 ml of 4 N sodium hydroxide solution are added and the mixture is heated for a further 12 hours to 60° C. It is then evaporated down in vacuo, the residue is taken up in water and the pH is adjusted to 5 by the addition of 4 N hydrochloric acid. It is extracted 5 times with dichloromethane/isopropanol 4:1 and the combined organic phases are dried on magnesium sulphate. The solvents are eliminated in vacuo and the product thus obtained is further reacted directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08686022B2 |
|---|
| Source dataset | uspto-grants-2014_04 |
|---|
| ORD ID | ord-a4b73d554071474aaacfce242f1c4804 |
|---|
| Source note | uspto-grants-2014_04 |
|---|