HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → HCID 59718039, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 59717988 | HCID 59717988 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 59718039 | HCID 59718039 | — |
Reaction Steps
To a solution of 5-benzoylamino-naphthalene-1-sulfonyl chloride 44 (0.1 g, 0.29 mmol) in dichloromethane (0.5 mL) was added triethylamine (0.06 ml, 0.43 mmol) and p-anisidine (0.05 g, 0.3 mmol). The resultant solution stirred at room temperature for 3 hours. The reaction mixture was quenched with water and the compound extracted into ethyl acetate. The organic extracts were washed with brine, dried over MgSO4, filtered and concentrated to provide the crude product as a yellow oil. 1H NMR (300 MHz, DMSO) δ 8.65 (d, 1H), 8.19 (d, 1H), 8.06 (m, 3H), 7.70 (m, 2H), 7.54 (m, 2H), 6.84 (d, 2H), 6.69 (d, 2H), 3.56 (s, 3H); LC/MS (M+H)+ m/z 433.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063222B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-0c9f3839e8574c5ea61e4357454e6562 |
| Source note | uspto-grants-2011_11 |