HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399629Generated: October 31, 2026
Triethylamine → 4-(2,4-dichlorophenyl)-5-methyl-2-[N-(alpha-cyclopropyl-4-bromobenzyl)-N-propylamino]thiazole
https://huagongshe.com/reaction/399629
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-1-(2,4-dichlorophenyl)propan-1-one | HCID 10923991 | — |
| Reactant | N-(alpha-cyclopropyl-4-bromobenzyl)-N-propylthiourea | HCID 18967805 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(2,4-dichlorophenyl)-5-methyl-2-[N-(alpha-cyclopropyl-4-bromobenzyl)-N-propylamino]thiazole | HCID 15291608 | — |
Reaction Steps
14 g of 2-bromo-1-(2,4-dichlorophenyl)-1-propanone (Compound 1), 17.1 g of N-(α-cyclopropyl-4-bromobenzyl)-N-propylthiourea (Compound 64) and 7.6 ml of triethylamine are dissolved in 200 ml of ethanol and the solution is heated to 65° C. The reaction is monitored by TLC. At the end of the reaction, the ethanol is removed and the residue is hydrolysed with water and extracted with methylene chloride. The organic phases are washed and dried. The product is purified on a column of silica, using a mixture of cyclohexane and ethyl acetate (20:1 v/v) as eluent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05821255 |
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| Source dataset | uspto-grants-1998_10 |
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| ORD ID | ord-41160342b3da4f80b92077bc9f490998 |
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| Source note | uspto-grants-1998_10 |
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