HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → HCID 9966080, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 21873976 | HCID 21873976 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 9966080 | HCID 9966080 | 87.4% |
Reaction Steps
1 g of 2,3-dimethyl-9-(3-thienyl)-7,8,9,10-tetrahydroimidazo[1,2-h][1,7]naphthyridin-7-one, suspended in 10 ml of methanol, is treated with 500 mg of sodium borohydride, the solvent is stripped off in vacuo after stirring at room temperature for 1 hour, the yellowish residue is treated with saturated aqueous ammonium chloride solution (100 ml) and the mixture is extracted three times with methylene chloride. The combined organic phases are washed with a little water, dried over sodium sulfate and the solvent is stripped off in vacuo. The remaining solid residue is stirred with a little (15 ml) diethyl ether and then filtered off. 0.88 g of the title compound of m.p. 192–94° C. (diethyl ether) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07141567B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-05185e17c0d249ee9ee205c689dd2cbe |
| Source note | uspto-grants-2006_11 |