HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850802Generated: October 30, 2026
1,2-Dichloroethane → HCID 66562026, compound
https://huagongshe.com/reaction/1850802
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 3-Fluoroazetidine | HCID 3603542 | — |
| Reactant | HCID 70856015 | HCID 70856015 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66562026 | HCID 66562026 | — |
Reaction Steps
The mixture of [6-(2-{(1S,2R)-2-[1-(3-isopropyl-1,2,4-oxadiazol-5-yl)piperidin-4-yl]cyclopropyl}ethoxy)-5-methylpyridin-3-yl]acetic acid (25 mg, 0.058 mM), 3-floroazetidine (8.7 mg, 0.116 mmol), EDC (17 mg, 0.087 mmol), HOBt (13 mg. 0.087 mmol) and triethyl amine (33 μL, 0.232 mmol) in 2 mL of DCM was stirred for 16 hrs at room temperature. The volatiles were then removed in vacuo and the residue was dissolved in CH3CN and water (1/1, 1.5 ml) and submitted to the Rahway High Throughput Purification Group to be purified. The HTP group used an HP mass-directed LC eluting with a gradient of 20-80% acetonitrile in water with 0.05% formic acid buffer to purify the compound. The desired product was obtained with 97.5% purity measured via Gilson HPLC analytical analysis. LCMS (ESI) m/z 486 [M+H]+. GPR119 Human EC50: 8 nM
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08957062B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-de18a018f7c04f7ea3f0176b837c6b39 |
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| Source note | uspto-grants-2015_02 |
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