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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 747259Generated: October 29, 2026

Trifluoroacetic acid → HCID 178420122, compound

https://huagongshe.com/reaction/747259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
Reactantbenzo[1,2,5]thiadiazol-4-yl-(1-trityl-1H-imidazol-4-yl)-methanoneHCID 59749576—
SolventDichloromethaneHCID 6344—
ProductHCID 178420122HCID 178420122—

Reaction Steps

A solution of benzo[1,2,5]thiadiazol-4-yl-(1-trityl-1H-imidazol-4-yl)-methanone (Intermediate L3) (500 mg, 1.12 mmol) in methylene chloride (2 mL) was treated with triethylsilane (8 mL), and trifluoroacetic acid (8 mL) at rt for 48 h. This mixture was evaporated under vacuum and quenched with a ˜7M NH3-MeOH solution. The solvent was exchanged with CH2Cl2. The solution was concentrated onto silica gel and purified by chromatography, eluting with 3% NH3-MeOH:CH2Cl2 to give 4-(1H-imidazol-4-ylmethyl)-benzo[1,2,5]thiadiazole (Intermediate L4). 4-(1H-imidazol-4-ylmethyl)-benzo[1,2,5]thiadiazole (Intermediate L4) was subjected to the appropriate process steps in Method A to produce 4-benzo[1,2,5]thiadiazol-4-ylmethyl-1,3-dihydro-imidazole-2-thione (Compound 16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07396849B2
Source datasetuspto-grants-2008_07
ORD IDord-8811cdac01ae48c58ecf1a519ed95e3c
Source noteuspto-grants-2008_07