HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1178004Generated: November 2, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 59559649, compound
https://huagongshe.com/reaction/1178004
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 4-(Benzyloxy)benzoic acid | HCID 73880 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 66953605 | HCID 66953605 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 59559649 | HCID 59559649 | 48.2% |
Reaction Steps
DIPEA (131 mg, 0.17 mL, 0.76 mmol) was added to a stirred solution of 4-Benzyloxy-benzoic acid (58 mg, 0.25 mmol) in DMF (2 mL). HOBT (41 mg, 0.3 mmol) and EDCI (58 mg, 0.3 mmol) were then added at room temperature. After 2 minutes, 2-amino-1-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-propan-1-one (85 mg, 0.25 mmol) was added and the resulting mixture was stirred at room temperature overnight. Cold water was then added and the product was extracted with EtOAc and the organic layer was washed with brine. The organic phase was dried over Na2SO4 and concentrated under reduced pressure to get the residue. The obtained residue was purified by column chromatography (using 60-120 silica gel and 10% MeOH in CHCl3 as eluent) to afford 65 mg (47% yield) of 4-benzyloxy-N-{1-methyl-2-oxo-2-[4-(2-trifluoromethyl-benzoyl)-piperazin-1-yl]-ethyl}-benzamide. LCMS Purity: 95%. 1H NMR (CDCl3): δ 7.76 (m, 3H), 7.6 (m, 2H), 7.4-7.3 (m, 5H), 7.1 (d, 1H), 7.0 (d, 2H), 5.22 (s, 2H), 4.2 (d, 1H), 3.82 (m, 2H), 3.7-3.4.(m, 6H), 2.0 (m, 1H), 1.4 (dd, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07842696B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-4fc9978781f2421da258fdabffe976e7 |
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| Source note | uspto-grants-2010_11 |
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