HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904515Generated: October 30, 2026
Chlorotrimethylsilane → HCID 178438394, compound
https://huagongshe.com/reaction/904515
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | Imidazolate | HCID 3386966 | — |
| Reactant | HCID 12862352 | HCID 12862352 | — |
| Reactant | HCID 178509300 | HCID 178509300 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178438394 | HCID 178438394 | — |
Reaction Steps
5.77 g (0.02 mol) of 4-oxo-2-propyl-4H-pyrido[1,2-a]thieno[2,3-d]pyrimidine-7-carboxylic acid (Example 3) and 6.49 g (0.04 mol) of 1,1'carbonyldiimidazole (Aldrich Chemical Company) in 100 ml of dimethylformamide are stirred at 50° C. for one hour. To 2.5 g (0.024 mol) of 5-aminotetrazole monohydrate (Aldrich Chemical Company) in 50 ml of dimethylformamide cooled to 0°-5° C. is added 9.14 ml (0.072 mol) of chlorotrimethylsilane (Aldrich Chemical Company) and 10 ml (0.072 mol) of triethylamine. The mixture is stirred and allowed to reach room temperature. After two hours the mixture is combined with the previous imidazolide mixture and stirred for fourteen hours at room temperature. The resulting precipitate 0.9 g, of 4-oxo-2-propyl-N-1H-tetrazol-5-yl-4H-pyrido[1,2-a]thieno[2,3-d]pyrimidine-7-carboxamide is collected; mp 306°-308° C. (dec) after recrystallization from pyridine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04230707 |
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| Source dataset | uspto-grants-1980_10 |
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| ORD ID | ord-a8db5dc344c741f397a2d54e96d0461c |
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| Source note | uspto-grants-1980_10 |
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