HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18536835, compound → HCID 18536936, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18536835 | HCID 18536835 | — |
| Reactant | HCID 18537002 | HCID 18537002 | — |
| Product | HCID 18536936 | HCID 18536936 | 91% |
Reaction Steps
5-(Methoxyphenylthio)-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxamidine: Methyl 5-(methoxyphenylthio)-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxylate (100 mg, 0.22 mmol) was treated in a manner similar to that for Example 10, step (b), to give 5-methoxy-4-(4-phenyl(1,3-thiazol-2-yl))thiophene-2-carboxamidine (94 mg, 91%) as an orange solid. 1H-NMR (DMSO-d6; 300 MHz) δ 9.49 (br s, 2H), 9.15 (br s, 2H), 8.70 (s, 1H), 8.26 (s, 1H), 8.07 (m, 2H), 7.49 (m, 2H), 7.40 (m, 1H), 7.35 and 6.90 (AB quartet, 2H, J=8.7 Hz), 4.41 (s, 2H), 3.73 (s, 3H). Mass spectrum (MALDI-TOF, CHCA matrix, m/z): Calcd. for C22H19N3OS3 438.5 (M+H), found 438.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06403633B2 |
| Source dataset | uspto-grants-2002_06 |
| ORD ID | ord-8aaf8407fdca43498364930acdfcde20 |
| Source note | uspto-grants-2002_06 |