Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium thiocyanateHCID 516872—
ReactantMethyl 4-amino-3-methoxybenzoateHCID 602411—
CatalystCopper SulfateHCID 24462—
SolventMethanolHCID 887—
ProductMethyl 2-amino-4-methoxybenzo[d]thiazole-6-carboxylateHCID 5956026984%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07842713B2
Source datasetuspto-grants-2010_11
ORD IDord-62dbd3c4ccf24a029e1a0128ada9c01e
Source noteuspto-grants-2010_11