HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfoxide → Methyl 3-cyclohexyl-2-(2-formyl-4-methoxyphenyl)-1-prop-2-yn-1-yl-1H-indole-6-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Methyl 3-cyclohexyl-2-[2-(hydroxymethyl)-4-methoxyphenyl]-1-prop-2-yn-1-yl-1H-indole-6-carboxylate | HCID 86637863 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-cyclohexyl-2-(2-formyl-4-methoxyphenyl)-1-prop-2-yn-1-yl-1H-indole-6-carboxylate | HCID 86637864 | — |
Reaction Steps
Oxalyl chloride (2.5 eq., 2M solution in DCM) was added at −70° C. under nitrogen atmosphere over a solution of DMSO (5 eq.) in anhydrous DCM and the mixture was stirred for 30 min; a solution of methyl 3-cyclohexyl-2-[2-(hydroxymethyl)-4-methoxyphenyl]-1-prop-2-yn-1-yl-1H-indole-6-carboxylate in DCM was then added and stirring was continued at the same temperature for 30 min. before NEt3 (8 eq.) was added. After stirring at 0° C. for 20 min. the mixture was diluted with DCM, washed with water, 1N HCl, saturated aq. NaHCO3 solution and brine. The organic phase was dried over Na2SO4 and evaporated in vacuo. The obtained yellow solid was used in the next step without purification. MS (ES+): 430.5 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08232390B2 |
| Source dataset | uspto-grants-2012_07 |
| ORD ID | ord-90833dcb6db043a785b14910492a3482 |
| Source note | uspto-grants-2012_07 |