HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-benzimidazole-5-carbohydrazide → HCID 178492804, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-benzimidazole-5-carbohydrazide | HCID 16637119 | — |
| Reactant | HCID 178492809 | HCID 178492809 | — |
| Product | HCID 178492804 | HCID 178492804 | — |
Reaction Steps
The compound was synthesized starting from benzimidazol-5-carbohydrazide (176 mg, 1 mmol) and 3,4-dimethoxyphenylsulfonylthioacetic acid (261 mg; 1 mmol) as described in method 2 but purified by flash chromatography on silica using a CHCl3/MeOH gradient; yield: 0.022 g (5.5%); MS m/z: 401.2 [M+H]+; 1H-NMR (DMSO d6, 400 MHz): δ 3.75 (s, 3H); 3.82 (s, 3H); 5.29 (s, 2H); 7.15 (d, 1H3J=8.7 Hz); 7.328-7.333 (m, 1H); 7.38 (dd, 1H, 4J=2.1 Hz, 3J=8.7 Hz); 7.68-7.72 (m, 1H); 7.78-7.82 (m, 1H); 8.01 (br s, 1H); 8.38 (s, 1H); 12.80 (br s, 1H); HPLC (METHOD [A]): rt 10.19 min (90.6%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09181233B2 |
| Source dataset | uspto-grants-2015_11 |
| ORD ID | ord-81fe628556db40a9a54c5a0117afd307 |
| Source note | uspto-grants-2015_11 |