HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455007Generated: October 30, 2026
Dimethylformamide → HCID 178509323, compound
https://huagongshe.com/reaction/455007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 43367333 | HCID 43367333 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178509323 | HCID 178509323 | 10% |
Reaction Steps
Starting material 12 (1.6 g, 6.4 mmol) was dissolved in 20 ml DMF. Then EDCl (1.46 g, 7.6 mmol) and HOBt (1.3 g, 9.5 mmol) were added. Now, one half of 1.04 g (6.4 mmol) 1H-1,2,3-benzothiazole-5-carboxyllic acid was added. The reaction mixture was stirred at ambient temperature over night. Then the other half of the 1H-1,2,3-benzothiazole-5-carboxyllic acid was added and the reaction mixture was again stirred at ambient temperature over night. The reaction mixture was now concentrated in vacuo yielding 7 g crude product. Those were taken up in ethyl acetate and water and the phases were separated. The organic phase was washed with water and the combined aqueous phases were washed with ethyl acetate. The combined organic phases were washed with brine, dried over MgSO4 and concentrated in vacuo. The desired product 13 was isolated as a brown oil (1.2 g, 20% content, 10% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497283B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-9d830e20e328417ca6f98e032eda3293 |
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| Source note | uspto-grants-2013_07 |
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