HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1355591Generated: October 30, 2026
1,2-Dichloroethane → HCID 131723948, compound
https://huagongshe.com/reaction/1355591
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 2,4,6-Trimethylpyridine | HCID 7953 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 87354904 | HCID 87354904 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 131723948 | HCID 131723948 | 108.4% |
Reaction Steps
A solution of compound 4 (150 mg, 0.51 mmol), 4-(aminomethyl)benzylnitrile (compound 6, 171 mg, 1.02 mmol), EDC (195 mg, 1.02 mmol), and N-hydroxybenzotriazole (78 mg, 0.51 mmol) in acetonitrile (5.1 ml) was stirred at ambient temperature for 10 minutes. 2,4,6-Collidine (0.34 ml, 2.54 mmol) was then added and the reaction mixture was stirred overnight at ambient temperature. The solvent was removed under reduced pressure and the resulting residue was resuspended in ethylacetate (100 ml) and 0.5M HCl (10 ml). The ethylacetate layer was washed with water followed by 0.5M HCl (10 ml), saturated sodium bicarbonate (2×10 ml) and brine (15 ml), then dried with sodium sulfate. The solvent was removed under reduced pressure to yield 237 mg product. The product eluted at 9.5 minutes by reverse phase (C18) HPLC at 0.11 trifluoroacetic acid in 5-75% aqueous acetonitrile over 20 minutes.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06586405B2 |
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| Source dataset | uspto-grants-2003_07 |
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| ORD ID | ord-38f9fd05fe11465a842754353da7fa80 |
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| Source note | uspto-grants-2003_07 |
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