HuagongsheHuagongshe Chemistry Print Report · For research reference only
(quinolin-3-yl)thiourea → HCID 18536962, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (quinolin-3-yl)thiourea | HCID 1480927 | — |
| Reactant | Methyl 5-methylthio-4-[2-(3-quinolylamino)(1,3-thiazol-4-yl)]thiophene-2-carboxylate | HCID 18536963 | — |
| Reactant | Methyl 4-(2-bromoacetyl)-5-methylthiothiophene-2-carboxylate | HCID 86583828 | — |
| Product | HCID 18536962 | HCID 18536962 | 78% |
Reaction Steps
Methyl 5-methylthio-4-[2-(3-quinolylamino)(1,3-thiazol-4-yl)]thiophene-2-carboxylate: Methyl 4-(2-bromoacetyl)-5-methylthiothiophene-2-carboxylate (90 mg, 0.28 mmol) was allowed to react with amino(3-quinolylamino)methane-1-thione (59.1 mg) as described in Example 154, step (a) to give 107.5 mg (78% yield) of methyl 5-methylthio-4-[2-(3-quinolylamino)(1,3-thiazol-4-yl)]thiophene-2-carboxylate hydrobromide. 1H NMR (DMSO-d6, 300 MHz) δ 2.75 (s, 3H), 3.84 (s, 3H), 7.52 (s, 1H), 7.92-8.05 (m, 2H), 8.22 (s, 1H), 9.22 (m, 2H); Mass Spectrun (ESI) m/z calcd. for C19H15N3O2S3, 413.54 (M+H), found 414.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562840B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-3ee2a2b6b51947d69526f9ab4fd4894e |
| Source note | uspto-grants-2003_05 |