HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257853Generated: October 26, 2026
Dicyclohexylcarbodiimide → N-[4-(4-ethylthiophenoxy)benzyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide
https://huagongshe.com/reaction/257853
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Dimethyl-1,3-oxazole-5-carboxylic acid | HCID 1132979 | — |
| Reactant | 4-(4-Ethylthiophenoxy)benzylamine | HCID 117033199 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-(4-ethylthiophenoxy)benzyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide | HCID 131718251 | 40.7% |
Reaction Steps
To a stirred mixture of 2,4-dimethyl-1,3-oxazole-5-carboxylic acid (155 mg, 1.1 mM) and dichloromethane (20 ml) was added 1,3-dicyclohexylcarbodiimide (227 mg, 1.1 mM) at 0°-10° C., and the mixture was stirred for 30 min at the same temperature. To this was added dropwise a solution (10 ml) of 4-(4-ethylthiophenoxy)benzylamine (285 mg, 1.1 mM) in dichloromethane, and the mixture was stirred for 12 h at room temperature. The mixture was poured into ice water, and the mixture was extracted with dichloromethane. The extract was washed with saturated ammonium chloride solution and brine, dried with magnesium sulfate, and concentrated in vacuo. The residue was chromatographed over silica gel to give N-[4-(4-ethylthiophenoxy)benzyl]-2,4-dimethyl-1,3-oxazole-5-carboxamide (164 mg, 39%) as colorless crystals, m.p. 60.0°-64.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05264448 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-9bf5f7adc5fd40939760c7953f06fb16 |
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| Source note | uspto-grants-1993_11 |
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