HuagongsheHuagongshe Chemistry Print Report · For research reference only
(NE)-N-(3-chloro-4-oxonaphthalen-1-ylidene)naphthalene-2-sulfonamide → (NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]-4-phenylbenzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (NE)-N-(3-chloro-4-oxonaphthalen-1-ylidene)naphthalene-2-sulfonamide | HCID 24282891 | — |
| Reactant | (NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]-4-phenylbenzenesulfonamide | HCID 46908285 | — |
| Product | (NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]-4-phenylbenzenesulfonamide | HCID 46908285 | 92.6% |
| Product | (NE)-N-[3-(1-methyltetrazol-5-yl)sulfanyl-4-oxonaphthalen-1-ylidene]naphthalene-2-sulfonamide | HCID 46908380 | — |
Reaction Steps
(E)-N-(3-(1-methyl-1H-tetrazol-5-ylthio)-4-oxonaphthalen-1(4H)-ylidene)naphthalene-2-sulfonamide (13ab) was prepared according to the procedure for 13x except using 12f, affording 85.5 mg (92.6%) title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08466157B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-cbd343fae8224585a8aa5ccd83f14b49 |
| Source note | uspto-grants-2013_06 |