HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro- → Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro- | HCID 796366 | — |
| Reactant | 4-[(2-Nitro-benzenesulfonylamino)-methyl]-benzoic acid tert-butyl ester | HCID 69794415 | — |
| Product | Benzenesulfonamide, N-[(4-methoxyphenyl)methyl]-2-nitro- | HCID 796366 | — |
| Product | 2-amino-N-(4-methoxy-benzyl)-benzenesulfonamide | HCID 1133991 | — |
Reaction Steps
When in the procedure of Example 17, Step (2), 4-[(2-nitro-benzenesulfonylamino)-methyl]-benzoic acid tert-butyl ester was replaced with N-(4-methoxy-benzyl)-2-nitro-benzenesulfonamide, the title compound 2-amino-N-(4-methoxy-benzyl)-benzenesulfonamide was obtained as a thick oil. 1H-NMR (CDCl3); δ 7.71 (dd, 1H), 7.07 (d, 2H), 6.78 (m, 4H), 4.93 (bt, 1H), 4.82 (bs, 2H), 3.95 (d, 2H), and 3.75 (s, 3H). MS: M+−1=291.0 Da Step (3): Synthesis of 2-Amino-5-bromo-N-(4-methoxy-benzyl)-benzenesulfonamide
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06849648B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-a1c0cd5e0a54433c8c51fba9e71b84e4 |
| Source note | uspto-grants-2005_02 |