HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → HCID 66966216, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 66966846 | HCID 66966846 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 66966216 | HCID 66966216 | 88% |
Reaction Steps
A solution of (S)-(E)-3-(10-oxo-2,3,4,9,10,10a-hexahydro-1H-3a,8,9-triaza-benzo[f]azulen-6-yl)acrylic acid tert-butyl ester (0.65 g, 1.97 mmol) in CH2Cl2 (7 mL) was treated with TFA (7 mL). After stirring at room temperature for 30 min, the clear tan solution was concentrated in vacuo. The resulting oil was treated with anhydrous dioxane (20 mL of a 4.0 M solution in dioxane, 80 mmol). The resulting mixture was sonicated for 5 min, stirred under N2 for 5 min and diluted with Et2O. The solid was isolated by filtration, suspended in Et2O, concentrated to dryness, and dried under vacuum overnight to give the title compound (0.60 g, 88%) as an off-white solid: MS (ESI) m/e 274 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07790709B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-e5cc84bd66324002ae9afbab4d43840f |
| Source note | uspto-grants-2010_09 |