HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708940Generated: November 1, 2026
Dimethylformamide → HCID 178433217, compound
https://huagongshe.com/reaction/1708940
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Methyl-1,3-thiazol-4-amine | HCID 14772700 | — |
| Reactant | HCID 178524966 | HCID 178524966 | — |
| Solvent | Benzene | HCID 241 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178433217 | HCID 178433217 | 41.1% |
Reaction Steps
A mixture, obtained by adding dry DMF(0.43 ml, 5.55 mmol) and then thionyl chloride (0.405 ml, 5.55 mmol) to dry benzene (1 ml) under ice-cooling, was allowed to warm up to room temperature and to react for 10 minutes upon which the mixture separated into two layers. The lower layer was added dropwise to dipotassium salt of 1H-tetrazole-5-carboxylic acid (704 mg, 3.70 mmol) suspended in dry acetonitrile (9 ml) under ice-cooling, and the mixture was allowed to react for 15 minutes. After adding dropwise a mixed solution of 2-methyl-4-thiazolamine (447.8 mg, 3.92 mmol) in dry acetonitrile (5 ml) and dry pyridine (1 ml) under the same conditions, the mixture was allowed to warm up to room temperature and to react for 1 hour. To the reaction mixture was added water, and the insoluble solids was removed by filtration and the filtrate was acidified with ice-cooled 2N HCl to pH 2. The precipitates were filtered, washed with water, and recrystallized from DMF-water to give yellowish crystals (320 mg, yield 41%) of N-(2-methyl-4-thiazolyl)-1H-tetrazole-5-carboxamide (Ia-1), m.p. 295°-297° C. (decomp).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04946855 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-e7e64689e0ab4069ab351ff678b63b39 |
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| Source note | uspto-grants-1990_08 |
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