HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Naphthalenesulfonyl chloride → Methyl 4-[(2-naphthalenylsulfonyl)amino]butanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Naphthalenesulfonyl chloride | HCID 7125 | — |
| Reactant | Methyl 4-aminobutanoate | HCID 18614 | — |
| Product | Methyl 4-[(2-naphthalenylsulfonyl)amino]butanoate | HCID 4204457 | 94% |
Reaction Steps
Using an analogous procedure to that described in Example 2, 2-naphthylsulphonyl chloride was reacted with methyl 4-aminobutyrate to give methyl 4-(2-naphthalenesulphonamido)butyrate in 94% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06730672B2 |
| Source dataset | uspto-grants-2004_05 |
| ORD ID | ord-06d98ad2281d4fe599fd82d0211ff84d |
| Source note | uspto-grants-2004_05 |