Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | HCID 15231545 | HCID 15231545 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 15231549 | HCID 15231549 | — |
Reaction Steps
0.52 g of the compound obtained in Example 5 step B), 25 ml of DCM and 0.5 g of pyridine were mixed. 0.54 ml of chloroacetyl chloride in 10 ml of DCM was then added over 5 minutes at 20° C. The reaction mixture was stirred for 2 hours at 20° C. and then concentrated under vacuum at 20° C. The residue was extracted with AcOEt and washed with water, then with 1N hydrochloric acid and then with water. It was dried over sodium sulfate and the solvent was evaporated off to give the expected product, which crystallized from isopropyl ether. m=0.6 g. M.p.=232° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05585394 |
|---|
| Source dataset | uspto-grants-1996_12 |
|---|
| ORD ID | ord-7d8ab79458c64a128ff7a27d7cb75e6a |
|---|
| Source note | uspto-grants-1996_12 |
|---|