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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298617Generated: October 30, 2026

2-Bromo-1,2-diphenylethan-1-one → HCID 86758672, compound

https://huagongshe.com/reaction/2298617

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-1,2-diphenylethan-1-oneHCID 102630—
ReactantMethyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylateHCID 86583815—
ProductHCID 86758672HCID 86758672—

Reaction Steps

A solution of 75 mg (0.3 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate (Maybridge, Cornwall, UK) was reacted with 92 mg, 0.3 mmol) of 2-bromo-1,2-diphenylethan-1-one in a manner similar to Example 8, step (a) to give, after preparative thin-layer chromatrography purification, methyl 4-(4,5-diphenyl(1,3-thiazol-2-yl))-5-methylthiothiophene-2-carboxylate (9 mg, 7%) as a solid. 1H-NMR (DMSO-d6; 300 MHz) δ8.94 (br s, 0.4H), 8.66 (s, 1H), 8.60 (br s, 0.3 H), 8.08 (s, 1H), 7.93 and 7.20 (AB quartet, 2H, J=8.7 Hz), 7.68 and 7.35 (AB quartet, 2H, J=8.2 Hz), 2.77 (s, 3H), ), 2.33 (s, 3H). Mass spectrum (MALDI-TOF, CHCA matrix, m/z): Calcd. for C22H17NO2S3, 424.0 (M+H), found 424.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492403B1
Source datasetuspto-grants-2002_12
ORD IDord-2c9e608e70e64520b0bac7765a7eed72
Source noteuspto-grants-2002_12