HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807978Generated: October 30, 2026
Sodium Bicarbonate → 3-[(2-Azido-4-methyl-cyclohexanecarbonyl)-isopropyl-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester
https://huagongshe.com/reaction/1807978
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Methyl 3-(isopropyl-amino)-5-phenylthiophene-2-carboxylate | HCID 11737447 | — |
| Reactant | 4-Methylcyclohex-1-ene-1-carbonyl chloride | HCID 18794966 | — |
| Reactant | 2-Azido-4-methyl-cyclohexanecarboxylic acid chloride | HCID 59752392 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-[(2-Azido-4-methyl-cyclohexanecarbonyl)-isopropyl-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester | HCID 59752394 | 49% |
Reaction Steps
To a solution of 3-Isopropylamino-5-phenyl-thiophene-2-carboxylic acid methyl ester (227 mg, 0.824 mmol) in 1,2-dichloroethane (2.5 ml) was added the 2:1 mixture of 2-Azido-4-methyl-cyclohexanecarboxylic acid chloride and 4-Methyl-cyclohex-1-enecarboxylic acid chloride (182 mg, 0.906 mmol) dissolved in 1,2-dichloroethane (0.5 ml). The resulting solution was stirred for 18 h at 90° C. and then cooled to room temperature. It was then diluted with ethyl acetate (10 ml) and a solution of saturated NaHCO3 (10 ml). The aqueous phase was separated and washed with ethyl acetate (2×10 ml) and the combined organic layers were dried (Na2SO4), filtered and concentrated. The residue was purified by flash chromatography (0% to 20% EtOAc/Hexane) to obtain 178 mg (49%) of 3-[(2-Azido-4-methyl-cyclohexanecarbonyl)-isopropyl-amino]-5-phenyl-thiophene-2-carboxylic acid methyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08357718B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-d24279c88df947a7b4274f3cdbebfd67 |
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| Source note | uspto-grants-2013_01 |
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