HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745396Generated: October 30, 2026
Diisopropylcarbodiimide → HCID 69585728, compound
https://huagongshe.com/reaction/1745396
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 1,2-Benzenedicarboxylic acid, 4-nitro- | HCID 69121 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 54228347 | HCID 54228347 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 69585728 | HCID 69585728 | — |
Reaction Steps
In a 4-ml scintillating vial, a solution of 2-amino-5-aminomethyl-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid tert-butyl ester (58 mg, 0.2 mmol) in tetrahydrofuran (2.0 ml) was treated with 4-nitrophthalic acid (63 mg, 0.3 mmol), diisopropylethylamine (190 μl, 1.1 mmol), and 1,3-diisopropylcarbodiimide (120 μl, 0.77 mmol). The reaction mixture was shaken vigorously for 10 seconds before being stirred at 50° C. for 43 hours and at room temperature for 20 hours. The solution was diluted with ethyl acetate (25 ml), washed with 0.5N aqueous hydrochloric acid (25 ml), saturated aqueous sodium bicarbonate (25 ml), and the brine (25 ml). The organic layer was dried (MgSO4), filtered and the solvent evaporated in vacuo. Crude 2-amino-5-(5-nitro-1,3-dioxo-1,3-dihydro-isoindol-2-ylmethyl)-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylic acid tert-butyl ester was obtained as a solid and used immediately in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07019026B1 |
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| Source dataset | uspto-grants-2006_03 |
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| ORD ID | ord-45fcd26aaee3473d941c5e5c36c19002 |
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| Source note | uspto-grants-2006_03 |
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