HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromopropionic acid → 3-[2-bromo-3-cyclohexyl-6-(methoxycarbonyl)-1H-indol-1-yl]propanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromopropionic acid | HCID 11553 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Methyl indole-6-carboxylate | HCID 639844 | — |
| Reactant | Methyl 2-bromo-3-cyclohexyl-1H-indole-6-carboxylate | HCID 11175076 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[2-bromo-3-cyclohexyl-6-(methoxycarbonyl)-1H-indol-1-yl]propanoic acid | HCID 68506143 | — |
Reaction Steps
NaH (3.5 eq, 60% dispersion in mineral oil) was added to a solution of methyl 2-bromo-3-cyclohexyl-1H-indole-6-carboxylate (prepared as described in WO 2004065367, from commercially available methyl indole-6-carboxylate) in DMF (0.2 M) and the solution allowed to stir at RT for 1 h. Then 3-bromopropanoic acid (1.1 eq) was added and the mixture stirred at RT for 2 h. DMF was concentrated in vacuo and the residue taken up in EtOAc. The organic phase was washed with 1 N HCl and then brine before being dried (Na2SO4), filtered and the solvent evaporated in vacuo. The title compound was used crude in the next step; MS (ES+) m/z 408 (M+H)+, m/z 410 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795247B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-11ca5de60f7b48ee9e99cd8be230424c |
| Source note | uspto-grants-2010_09 |