HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Ethyl Ketone → HCID 86739836, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Ethyl Ketone | HCID 6569 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Morpholine, 4-(2-chloroethyl)-, hydrochloride (1:1) | HCID 77210 | — |
| Reactant | HCID 2826591 | HCID 2826591 | — |
| Product | HCID 86739836 | HCID 86739836 | — |
Reaction Steps
2-(4-Chlorophenylmethylidene)-2H-1,4-benzothiazine-3(4H)-one (2.0 g) was reacted with sodium hydroxide (0.72 g) in methyl ethyl ketone (20 ml) at 80° C. for 30 minutes. After the solution turned clear, it was cooled to room temperature. N-(2-chloroethyl)morpholine hydrochloride (1.7 g) was added to the mixture. The organic solvent was evaporated under reduced pressure. The resulted yellow solid was filtered and washed with water and with methanol. It was recrystallized from a mixture of dimethylformamide and isopropyl alcohol. 2-(4-Chlorophenyl)-methylidene-4-(2-morpholinoethyl)-2H-1,4-benzothiazine-3(4H)-one (2.0 g) was obtained as yellow crystals, m.p. 173° to 175° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04490292 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-5ea74725cb7148baa5e7350714fafd96 |
| Source note | uspto-grants-1984_12 |