HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716822Generated: October 25, 2026
1,2-Dichloroethane → HCID 68666178, compound
https://huagongshe.com/reaction/1716822
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | L-Serine, methyl ester, hydrochloride (1:1) | HCID 2723730 | — |
| Reactant | 4-(1H-benzimidazol-1-ylmethyl)benzoic acid | HCID 2735444 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68666178 | HCID 68666178 | 64% |
Reaction Steps
A stirred solution of 4-[(1H-benzoimidazol-1-yl)methyl]benzoic acid (4 g, 15.87 mmol) in DMF at 0° C. is treated sequentially with EDC (3.6 g, 19 mmol), HOBt (2.5 g, 19 mmol), DIPEA (5.1 g, 39.5 mmol, 2.5 eq) and serine methyl ester hydrochloride (2.9 g, 19 mol), stirred at room temperature overnight and evaporated to dryness. The resultant residue is dissolved in EtOAc and water. The layers are separated and the organic layer is washed successively with 1M HCl, water, saturated NaHCO3 and brine, dried over Na2SO4 and concentrated under reduced pressure to give the title product in 64% yield, identified by NMR and mass spectral analyses. 1H NMR (400 MHz, DMSO-d6): 8.23-8.26 (m, 2H); 7.9 (s, 2H); 7.87 (d, J=7.6 Hz, 2H); 7.70 (d, J=6 Hz, 1H); 7.33 (m, 3H); 7.20 (m, 2H); 5.54 (s, 2H); 4.90 (t, J=4 Hz, 1H); 4.60 (m, 1H); 3.84-3.90 (m, 2H); 3.70 (s, 3H). LCMS (ESI+) 354 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07803825B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-d76db4cedc374c2890d60d1bc865e517 |
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| Source note | uspto-grants-2010_09 |
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