HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252075Generated: November 2, 2026
Dimethylformamide → 4-[4-(3-Indolyl)piperidinomethyl]-2-(2-acetoxyacetylamino)thiazole
https://huagongshe.com/reaction/1252075
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Acetoxyacetyl chloride | HCID 26297 | — |
| Reactant | 4-((4-(1H-Indol-3-yl)piperidin-1-yl)methyl)thiazol-2-amine | HCID 14129796 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-[4-(3-Indolyl)piperidinomethyl]-2-(2-acetoxyacetylamino)thiazole | HCID 14129799 | 17.4% |
Reaction Steps
To a mixture of 4-[4-(3-indolyl)piperidinomethyl]-2-aminothiazole (1 g), triethylamine (1.3 g) and N,N-dimethylformamide (10 ml) was added dropwise a solution of 2-acetoxyacetyl chloride (0.87 g) in methylene chloride (1 ml) in a stream of nitrogen gas with ice-cooling and stirring over a period of 20 minutes. After 3 hours, the reaction mixture was filtered and the residue on the filter paper was washed with N,N-dimethylformamide (10 ml). The filtrate and washings were combined and concentrated under reduced pressure to remove the solvent. The residue was subjected to column chromatography on silica gel and elution was carried out with a mixture of chloroform and methanol (20:1 V/V). The fractions containing the desired compound were collected and concentrated under reduced pressure and the residue was recrystallized from a mixture of water and ethanol to give 4-[4-(3-indolyl)piperidinomethyl]-2-(2-acetoxyacetylamino)thiazole (0.23 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04742057 |
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| Source dataset | uspto-grants-1988_05 |
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| ORD ID | ord-920ebc5f8f2f4d0991788163f1b23848 |
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| Source note | uspto-grants-1988_05 |
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