HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1360758Generated: November 1, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 25235303, compound
https://huagongshe.com/reaction/1360758
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1,1'-Thiocarbonyldiimidazole | HCID 80264 | — |
| Reactant | 3-Amino-4-picoline | HCID 137935 | — |
| Reactant | 2-(2,6-Dichloro-phenyl)-3H-benzoimidazole-5-carboxylic acid hydrazide | HCID 57786585 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 25235303 | HCID 25235303 | — |
Reaction Steps
Combine 3-amino-4-methyl-pyridine (66 mg, 0.606 mmol) and di-imidazol-1-yl-methanethione (108 mg, 0.606 mmol) in DMF (1.5 mL) and stir for 7.5 hr. Add 2-(2,6-dichloro-phenyl)-3H-benzoimidazole-5-carboxylic acid hydrazide (150 mg, 0.466 mmol) and DMF (1 mL). Stir for 3 days. Add EDCI (179 mg, 0.932 mmol) and heat to 80° C. for 1 hr. Upon cooling, dilute the reaction with EtOAc (75 mL) and extract with water (15 mL). Dry the organic phase over Na2SO4 and evaporate the solvent. Purify the residue by reverse phase HPLC (30-45% ACN/H2O+5 mM NH4OH) to afford the title compound as a light yellow solid: 1H NMR (400 MHz, DMSO-d6) δ ppm 2.35 (s, 3H) 7.30 (d, J=4.80 Hz, 1H) 7.62-7.68 (m, 1H) 7.72 (d, J=2.02 Hz, 1H) 7.70 (s, 1H) 7.83 (br. s., 2H) 7.98-8.19 (m, 1H) 8.24 (d, J=4.80 Hz, 1H) 8.98 (s, 1H) 9.95 (br. s., 1H) 13.28 (br. s., 1H); MS m/z=436.9 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07879850B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-70c46147a6c744fcb46208d4654c47d0 |
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| Source note | uspto-grants-2011_02 |
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