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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2102780Generated: November 1, 2026

Methylthiourea → 2-Methylamino-5,6-dihydro-4H-benzothiazol-7-one

https://huagongshe.com/reaction/2102780

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylthioureaHCID 2723704—
Reactant2-Bromocyclohexane-1,3-dioneHCID 2770476—
SolventPyridineHCID 1049—
Product2-Methylamino-5,6-dihydro-4H-benzothiazol-7-oneHCID 342749043%

Reaction Steps

A solution of 2-bromo-cyclohexane-1,3-dione (8.0 g, 41.9 mmol) and methyl thiourea (3.77 g, 41.9 mmol) in pyridine (63 mL) was stirred at room temperature for 16 h. The reaction mixture was concentrated under vacuum, extracted with CH2Cl2 /10% aq NaCl solution, dried, filtered, and concentrated under vacuum. Crystallization from EtOAc afforded the title compound as yellow crystals (3.26 g, 43%): mp 180-182° C. Anal. RP-HPLC: tR 8.4 min (0-60% MeCN, purity 100%). 1H-NMR (CDCl3): δ 7.90 (s, 1H, NH), 2.99 (s, 3H, CH3), 2.72 (t, 2H, J 6.1, CH2), 2.49 (t, 2H, J 6.1, CH2), 2.10 (qu, 2H, J 6.1, CH2). 13C-NMR (CDCl3): δ 191.0, 176.6, 168.0, 120.0, 37.5, 32.5, 27.7, 23.2. MS: (ESI+) m/z 183.07 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576091B2
Source datasetuspto-grants-2009_08
ORD IDord-3a878cd7311a4754a19f1aa0345b618a
Source noteuspto-grants-2009_08