HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chlorobutyryl chloride → HCID 66620109, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chlorobutyryl chloride | HCID 78370 | — |
| Reactant | 4-Chloro-1,5-naphthyridin-3-amine | HCID 66619961 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 66620109 | HCID 66620109 | — |
Reaction Steps
A mixture of 4-chloro[1,5]naphthyridin-3-amine (2.0 g, 11 mmol) and 4-chlorobutyryl chloride (4.7 g, 33 mmol) in 1,2-dichloroethane (75 mL) was heated at reflux for 20 hours. The reaction mixture was then concentrated under reduced pressure and the residue washed with two 25 mL portions of hexane. The solid was then taken up in methanol (35 mL), 1.0 mL of 10% solution of sodium hydroxide in water was added, and the solution was stirred at room temperature for 4 hours. The reaction mixture was then concentrated under reduced pressure to provide 4-chloro-N-(4-chloro[1,5]naphthyridin-3-yl)butanamide which was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088788B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-5f1d9f5421b444c0a23c14a28b7ac1db |
| Source note | uspto-grants-2012_01 |