HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → HCID 10517849, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 10612438 | HCID 10612438 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 10517849 | HCID 10517849 | — |
Reaction Steps
To a mixture of 7-[(benzyloxy)carbonyl]-7-azabicyclo[2.2.1]heptane-1-carboxylic acid (550 mg) produced above, N,N-dimethylformamide (0.02 mL) and tetrahydrofuran (10 mL) was added dropwise ethanedioyl dichloride (0.80 mL) at room temperature. The mixture was stirred at room temperature for 30 min, and the reaction system was concentrated under reduced pressure. To the residue was added a small amount of tetrahydrofuran, and the mixture was concentrated again under reduced pressure to give a crude product (2.0 mmol) of the title compound. The obtained crude product of the title compound was used for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08722660B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-8f33578780054a2baf00733c86124f8a |
| Source note | uspto-grants-2014_05 |