HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-Acetyl-5-phenylsulphonamido-1,2,3,4-tetrahydroisoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 1-(5-amino-3,4-dihydroisoquinolin-2(1H)-yl)ethanone | HCID 21271726 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Acetyl-5-phenylsulphonamido-1,2,3,4-tetrahydroisoquinoline | HCID 21271724 | 82.9% |
Reaction Steps
To a stirred solution of 2-acetyl-5-amino-1,2,3,4-tetrahydroisoquinoline (6.6 g) in a mixture of dry pyridine (3 g) and dichloromethane (450 ml) at approximately 5° C. was added dropwise, over 15 minutes, benzenesulphonyl chloride (6.2 g). The orange solution was stirred overnight at room temperature and was then washed several times with water, dried and the solvent was then evaporated to give a dark orange oil. Crystallisation from 2-propanol gave 2-acetyl-5-phenylsulphonamido-1,2,3,4-tetrahydroisoquinoline as a pale pink solid (9.5 g) m.p. 131°-132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04812573 |
| Source dataset | uspto-grants-1989_03 |
| ORD ID | ord-87293aca5f094c7ba142a0ccfef0d8d5 |
| Source note | uspto-grants-1989_03 |