HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 67437172, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67114485 | HCID 67114485 | — |
| Reactant | HCID 67436438 | HCID 67436438 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Thionyl Chloride | HCID 24386 | — |
| Product | HCID 67437172 | HCID 67437172 | 83% |
Reaction Steps
A mixture of trans-2-(5-fluoro-pyridin-2-yl)-cyclopropanecarboxylic acid HCl salt (217 mg, 1 mmol) in thionyl chloride (2 mL) was heated at reflux for over night. The mixture was concentrated and dried under high vacuum for 3 h. Then the residue was dissolved in DCM (4 mL) and added dropwise to a solution of ((1S,2S)-1-{[4-(t-butyl-dimethyl-silanyloxy)-phenylamino]-methyl}-2-methyl-butyl)-carbamic acid tert-butyl ester (422 mg, 1 mmol) and triethyl amine (409 uL, 3 mmol) in DCM (4 mL). The resulting mixture was stirred at rt for overnight. The reaction mixture was concentrated and the residue was subjected to ISCO (40 g column, 0-40% EtOAc in hexane over 40 min.) to give the titled compound (486 mg, 83%). MS (MH+ 586).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08426414B2 |
| Source dataset | uspto-grants-2013_04 |
| ORD ID | ord-bcefcbcc7e5f4a40b15c79565ac74744 |
| Source note | uspto-grants-2013_04 |