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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 332881Generated: October 30, 2026

Azidotrimethylsilane → HCID 178489231, compound

https://huagongshe.com/reaction/332881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAzidotrimethylsilaneHCID 78378—
Reactant(E)-3-(4-((6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl)oxy)phenyl)acrylamideHCID 86730663—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 178489231HCID 17848923188.2%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a microwave vial, (E)-3-(4-((6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl)oxy)phenyl)acrylamide (75 mg, 0.174 mmol) and Bu2SnO (4.33 mg, 0.02 mmol) were suspended in DME (3 mL). The vial was charged with TMSN3 (0.023 mL, 0.17 mmol) and the reaction was heated for 60 min at 180° C. under microwave irradiation. The reaction mixture was filtered to remove solids and concentrated onto silica gel. The crude material was purified by column chromatography (SiO2, 1-20% MeOH/DCM) to afford (E)-5-(4-((6-methoxy-2-(4-methoxyphenyl)benzo[b]thiophen-3-yl)oxy)styryl)-1H-tetrazole (66 mg, 0.15 mmol, 83% yield) as a white solid. 1H NMR (400 MHz, CD3OD) δ ppm=7.45-7.61 (m, 5H), 7.32 (d, J=2.02 Hz, 1H), 7.15 (d, J=9.09 Hz, 1H), 6.98 (d, J=16.67 Hz, 1H), 6.86-6.93 (m, 2H), 6.78-6.86 (m, 3H), 3.78 (s, 3H), 3.69 (s, 3H). LC/MS (m/z, MH+): 457.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877801B2
Source datasetuspto-grants-2014_11
ORD IDord-8125ed80152644fd8b57603bae911f9a
Source noteuspto-grants-2014_11