HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421966Generated: October 30, 2026
Dimethyl Sulfoxide → Methyl 13-cyclohexyl-6-formyl-6,7-dihydro-5H-indolo[2,1-a][2]benzazepine-10-carboxylate
https://huagongshe.com/reaction/421966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | methyl 13-cyclohexyl-6-(hydroxymethyl)-6,7-dihydro-5H-indolo[2,1-a][2]benzazepine-10-carboxylate | HCID 16072734 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 13-cyclohexyl-6-formyl-6,7-dihydro-5H-indolo[2,1-a][2]benzazepine-10-carboxylate | HCID 86640311 | — |
Reaction Steps
DMSO (5 eq.) was dissolved in DCM and the solution was cooled to −78° C. At this temperature a 2M solution of oxalylchloride in DCM (2.5 eq.) was added slowly and the mixture was left stirring for 25 min at −78° C. A solution of methyl 13-cyclohexyl-6-(hydroxymethyl)-6,7-dihydro-5H-indolo[2,1-a][2]benzazepine-10-carboxylate (1 eq.) in DCM (0.09M) was added slowly at −78° C. and stirring was continued for 25 min at this temperature. Then NEt3 (8 eq.) was added and the resulting slurry was placed into an ice bath at 0° C. The mixture was stirred for 90 min, then diluted with DCM and extracted with water, HCl 1N, sat. aq. NaHCO3 and brine. After drying over Na2SO4 all volatiles were evaporated in vacuo. After evaporation of the solvent the product was obtained as a yellowish solid (quant.). (ES+) m/z 402 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08101595B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-5a8b09bda8fb45bba391ba78e43cab5e |
|---|
| Source note | uspto-grants-2012_01 |
|---|