HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Nitrothiophene-2-carboxaldehyde → HCID 86587363, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Nitrothiophene-2-carboxaldehyde | HCID 78281 | — |
| Reactant | N1-bicyclo[2.2.1]hept-5-en-2-ylhydrazine-1-carbothioamide | HCID 2740681 | — |
| Product | HCID 86587363 | HCID 86587363 | — |
Reaction Steps
The title compound was prepared from a mixture of N1-bicyclo[2.2.1]hept-5-en-2-ylhydrazine-1-carbothioamide (100 mg, 0.56 mmol) and 5-nitrothiophene-2-carboxaldehyde (88 mg, 0.56 mmol) similar to Example 3 and isolated as an orange solid (67 mg, 37%). 1H NMR (CDCl3): 10.13 (s, 1H), 7.96 (s, 1H), 7.86 (d, J=4.2 Hz, 1H), 7.37 (d, J=7.5 Hz, 1H), 7.17 (d, J=4.2 Hz, 1H), 6.26-6.13 (m, 2H), 4.26-4.20 (m, 1H), 3.05 (s, 1H), 3.00 (s, 1H), 1.95-1.87 (m, 1H), 1.70 (d, J=9.0 Hz, 1H), 1.49 (d, J=9.0 Hz, 1H), 1.46-1.39 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794400B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-22adb07e2126445a93903e761cc6cc8b |
| Source note | uspto-grants-2004_09 |