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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1155865Generated: October 30, 2026

Chlorotrimethylsilane → HCID 178422238, compound

https://huagongshe.com/reaction/1155865

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantImidazolateHCID 3386966—
ReactantHCID 12862350HCID 12862350—
ReactantHCID 178509300HCID 178509300—
SolventDimethylformamideHCID 6228—
ProductHCID 178422238HCID 17842223829.5%

Reaction Steps

1.86 g (0.00715 mol) of 2-methyl-4-oxo-4H-pyrido[1,2-a]thieno[2,3-d]pyrimidine-7-carboxylic acid (Example 1) and 1.62 g (0.01 mol) of 1,1'carbonyldiimidazole (Aldrich Chemical Company) in 210 ml of dimethylformamide are stirred at 50° C. for sixteen hours. To 0.83 g (0.008 mol) of 5-aminotetrazole monohydrate (Aldrich Chemical Company) in 50 ml of dimethylformamide cooled to 0°-5° C. is added 3.0 ml (0.024 mol) of chlorotrimethylsilane (Aldrich Chemical Company) and 6.0 ml (0.043 mol) of triethylamine. After thirty minutes the mixture is allowed to reach room temperature and is stirred for an additional two hours. This mixture is combined with the previous cooled imidazolide mixture and stirred for three days at room temperature. The resulting precipitate is collected, slurried in boiling glacial acetic acid, the mixture is cooled and filtered to give 0.69 g of 2-methyl-4-oxo-N-1H-tetrazol-5-yl-4H-pyrido[1,2 -a]thieno[2,3-d]pyrimidine-7-carboxamide; mp 306°-310° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04332947
Source datasetuspto-grants-1982_06
ORD IDord-ccbf6f20a9ef4e74a04900ba8ceb95e4
Source noteuspto-grants-1982_06