HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-methanesulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 2,3,4,5-Tetrahydro-1H-benzo(d)azepine | HCID 1400243 | — |
| Reactant | 3-Acetyl-7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine | HCID 11265634 | — |
| Reactant | 3-acetyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7-sulfonyl chloride | HCID 11346737 | — |
| Product | 7-methanesulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride | HCID 21242879 | — |
Reaction Steps
Following the procedure of Examples 1 and 4, 2,3,4,5-tetrahydro-1H-3-benzazepine was converted to 3-acetyl-7-chlorosulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine and then to 3-acetyl-7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine which was hydrolyzed with hydrochloric acid to give 7-methylsulfonyl-2,3,4,5-tetrahydro-1H-3-benzazepine hydrochloride, m.p. 275°-277° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04824839 |
| Source dataset | uspto-grants-1989_04 |
| ORD ID | ord-fd83b138521e4376a4f73a18e9b7c44c |
| Source note | uspto-grants-1989_04 |