HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → HCID 178487802, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 178487805 | HCID 178487805 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178487802 | HCID 178487802 | 86.6% |
Reaction Steps
Trifluoroacetic acid (821 μL, 10.56 mmol, 15.0 eq) is added at 0° C. to a stirred solution of [trans-4-(8-methoxy-1,2-dihydro-3-oxa-5,9-diaza-cyclopenta[a]naphthalen-2-ylmethyl)-cyclohexyl]-carbamic acid tert-butyl ester (300 mg, 0.70 mmol, 1.0 eq) in dichloromethane (12 mL). After 2 hours stirring at room temperature, the reaction mixture is extracted with dichloromethane (3×10 mL) and water (10 mL) and the pH is adjusted to 12 by the addition of a 1N sodium hydroxide aqueous solution. The combined organic layers are dried over sodium sulfate, filtered and concentrated to afford trans-4-(8-methoxy-1,2-dihydro-3-oxa-5,9-diaza-cyclopenta[a]naphthalen-2-ylmethyl)-cyclohexylamine as an orange viscous oil (190 mg, 82% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321788B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-3dc1885ed42f4482afe6103137bb24b3 |
| Source note | uspto-grants-2016_04 |