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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1785507Generated: November 1, 2026

Trifluoroborane-methyl sulfide → HCID 23653658, compound

https://huagongshe.com/reaction/1785507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroborane-methyl sulfideHCID 11137191—
Reactant2-(5,6-Dimethoxybenzoimidazol-1-yl)-4-phenylthiazole-5-carboxylic acid ethyl esterHCID 24886662—
SolventDichloromethaneHCID 6344—
ProductHCID 23653658HCID 2365365890.4%

Reaction Steps

Boron trifluoride dimethylsulfide (4.1 ml, 39 mmol) was added in multiportions over 5 hrs. to a suspension of 2-(5,6-Dimethoxybenzoimidazol-1-yl)-4-phenylthiazole-5-carboxylic acid ethyl ester (2.04 g, 4.99 mmol) in methylene chloride at RT. The mixture was stirred for an additional 40 mins. Ice water was added. Methylene chloride was removed, the residue was filtered, the solid was washed with water and a small amount of methanol, and then dried in air to give the product (1.72 g, yield 90%). 1H-NMR (DMSO-D6) 8.72 (s, 1H); 8.78-8.88 (m, 2H); 7.64 (s, 1H); 7.42-7.51 (m, 3H); 7.08 (s, 1H); 4.22 (q, 2H), 1.22 (t, 3H). MS M/z 382 (M+1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07504513B2
Source datasetuspto-grants-2009_03
ORD IDord-ccc8952ed6af4a2db53bf5335c8373ae
Source noteuspto-grants-2009_03