HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 977185Generated: October 31, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 10711401, compound
https://huagongshe.com/reaction/977185
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | HCID 10544360 | HCID 10544360 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 10711401 | HCID 10711401 | 31.3% |
Reaction Steps
To a solution of 4-carboxymethoxy-7-chloro-3-phenyl--2(1H)-quinolone (0.93 g Example 15) in tetrahydrofuran (50 ml) under nitrogen at room temperature, was added triethylamine (1.90 ml), ammonium acetate (0.50 g), 1-hydroxybenzotriazole (0.60 g) and 1-(3 dimethylaminopropyl)-3-ethyl carbodiimide (0.90 g). The reaction mixture was stirred at room temperature for 3 days, then poured into water (100 ml) and extracted with ethyl acetate (3×50 ml). The combined organic layers were washed with 1N citric acid (1×75 ml), water (1×75 ml), saturated sodium hydrogen carbonate (1×75 ml) and brine (1×75 ml), then dried (MgSO4), filtered and the solvent was removed in vacuo to leave a solid residue. Recrystallisation from MeOH gave the title compound (0.29 g). Mp 262°-264° C. Found: C, 66.31; H, 5.95; N, 7.46; C19H19N2O2Cl 0.1C6H14 0.6H2O requires C, 65.97; H, 5.93; N, 7.85%. δ (360 MHz, DMSO-d6) 3.91 (2H, s, OCH2CONH2), 7.25-7.45 (9H, m, Ph+6H+8-H+OCH2CONH2), 8.01 (1H, d, J=8.66 Hz, 5-H), 11.92 (1H, bs, NH). m/z (CI+), 329, (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05614532 |
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| Source dataset | uspto-grants-1997_03 |
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| ORD ID | ord-70327acf8b0f43718dd48fef330b80b5 |
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| Source note | uspto-grants-1997_03 |
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