HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → methyl 4-({2-[1-benzhydryl-2-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5-chloro-1H-indol-3-yl]ethyl}sulfanyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl 4-sulfanylbenzoate | HCID 237573 | — |
| Reactant | 1-benzhydryl-3-(2-bromoethyl)-2-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5-chloro-1H-indole | HCID 70160579 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 4-({2-[1-benzhydryl-2-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5-chloro-1H-indol-3-yl]ethyl}sulfanyl)benzoate | HCID 70160847 | 81% |
Reaction Steps
1-benzhydryl-3-(2-bromoethyl)-2-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5-chloro-1H-indole (1 eq) was mixed with Methyl 4-mercaptobenzoate (2 eq) and KC2CO3 (1.9 eq) in DMF (0.09M). The resulting mixture was stirred at rt under N2 overnight. Water was then added, followed by regular work-up (eg. EtOAc extration, brine wash, etc) and column purification (1:6 EtOAc/Hexane as eluent) to give methyl 4-({2-[1-benzhydryl-2-({[tert-butyl(dimethyl)silyl]oxy}methyl)-5-chloro-1H-indol-3-yl]ethyl}sulfanyl)benzoate (yellow oil) in 81% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06500853B1 |
| Source dataset | uspto-grants-2002_12 |
| ORD ID | ord-3e55cba812464f8ebbb6230b40430770 |
| Source note | uspto-grants-2002_12 |