HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409049Generated: October 30, 2026
Diisopropylethylamine → HCID 136603191, compound
https://huagongshe.com/reaction/1409049
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 10517849 | HCID 10517849 | — |
| Reactant | 3-Amino-5-bromothiophene-2-carboxamide | HCID 21975862 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 136603191 | HCID 136603191 | — |
Reaction Steps
To a mixture of 3-amino-5-bromothiophene-2-carboxamide (221 mg) produced in Example 1, step D, the crude product (2.0 mmol) of benzyl 1-(chlorocarbonyl)-7-azabicyclo[2.2.1]heptane-7-carboxylate produced above and tetrahydrofuran (10 mL) was added N-ethyl-N-(1-methylethyl)propan-2-amine (0.70 mL) at room temperature. After stirring for 1 hr, the reaction system was poured into saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. To the residue were added ethanol (10 mL) and 2M sodium hydroxide (2.5 mL), and the mixture was stirred at 100° C. overnight. The reaction system was cooled to room temperature, poured into saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate/hexane and methanol/ethyl acetate) to give the title compound (313 mg) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08921354B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-1cb4ccb2ff1d4a098604f387661da89e |
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| Source note | uspto-grants-2014_12 |
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