HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1177349Generated: November 1, 2026
Potassium thiocyanate → Methyl 2-amino-4-methoxybenzo[d]thiazole-6-carboxylate
https://huagongshe.com/reaction/1177349
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Reactant | Methyl 4-amino-3-methoxybenzoate | HCID 602411 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Methyl 2-amino-4-methoxybenzo[d]thiazole-6-carboxylate | HCID 59560269 | 84% |
Reaction Steps
To a solution of methyl 4-amino-3-methoxybenzoate (307 g, 1.696 mol) in anhydrous methanol (4 L) was added an intimated mixture of KSCN (1640 g, 16.9 mol) and anhydrous CuSO4 (1350 g, 8.44 mol) in one portion. The mixture was heated to reflux for 4 h. TLC (EtOAc/Petroleum ether 1:4) showed the reaction was complete. The mixture was filtered and the filtrate was diluted with water. The solution was heated to boiling until a slightly clear solution formed. The mixture was cooled to ambient temperature and left standing for 1 day. A dark yellow solid was formed, which was collected by filtration to afford the desired product (338 g, 84%) as a dark yellow solid. 1H NMR (400 MHz, CDCl3): δ 9.000-8.200 (br, 2H), 8.052 (s, 1H), 7.435 (s, 1H), 3.927 (s, 3H), 3.827 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842713B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-62dbd3c4ccf24a029e1a0128ada9c01e |
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| Source note | uspto-grants-2010_11 |
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