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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 723953Generated: October 31, 2026

1-(2-Amino-benzothiazol-5-yl)-3-benzoyl-thiourea → N-(2-Amino-1,3-benzothiazol-5-yl)thiourea

https://huagongshe.com/reaction/723953

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Amino-benzothiazol-5-yl)-3-benzoyl-thioureaHCID 10042159—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductN-(2-Amino-1,3-benzothiazol-5-yl)thioureaHCID 10263051—

Reaction Steps

To a solution of anhydrous methanol (213 mL) was added sodium methoxide (1.15 g) and 1-(2-amino-benzothiazol-5-yl)-3-benzoyl-thiourea (Example 17, 3.5 g). The resulting mixture was stirred at room temperature for 3 hours. The mixture was concentrated and the residue was poured into water (300 mL). The mixture was extracted using ethyl acetate (3×200 mL). The combined organic fractions were dried over magnesium sulfate, filtered and concentrated (1.61 g, 67%). 1H-NMR (DMSO d6) δ: 9.64 (s, 1H), 760–7.37 (m, 6H), 6.96 (d, 1H, J=8.3 Hz); MS (ESI) 224.8 (M+1, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07141595B2
Source datasetuspto-grants-2006_11
ORD IDord-2d147e4a4f77402cb0359c7476e5289c
Source noteuspto-grants-2006_11