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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230008Generated: November 1, 2026

1,2-Dichloroethane → HCID 178481251, compound

https://huagongshe.com/reaction/230008

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantHydrochloric AcidHCID 313—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 68834955HCID 68834955—
ReactantHCID 178509300HCID 178509300—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178481251HCID 178481251—

Reaction Steps

To a solution of the title compound of Example 221 Step F (0.11 mmol, 50 mg), 1H-tetraazol-5-amine monohydrate (0.23 mmol, 24 mg), HOBt (0.29 mmol, 43 mg) and EDC (0.46 mmol, 88 mg) in 1 mL of DMF was added DIEA (0.57 mmol, 100 μL). The reaction mixture was allowed to stand at ambient temperature overnight, then poured into a mixture of dilute pH 7 buffer/EtOAc, which was acidified with 2 N HCl until two clear layers formed after agitation. The organic phase was concentrated under reduced pressure and the residue was purified by reverse-phase chromatography (Condition B) and lyophilized, affording a white solid. 1H NMR (500 MHz, DMSO) δ 8.06 (d, 2H), 7.68 (d, 2H), 7.55 (m, 2H), 7.42 (d, 2H), 7.34 (m, 2H), 7.20 (d, 2H), 6.18 (m, 1H), 5.38 (s, 2H), 3.31 (s, 3H), 2.35 (m, 2H), 2.18 (m, 2H), 1.73 (m, 2H), 1.60 (m, 2H). MS (ESI): m/z 505 (M+H). HPLC A: 1.99 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07563815B2
Source datasetuspto-grants-2009_07
ORD IDord-f1eaa9c0a37a4ebf924535b16094cd35
Source noteuspto-grants-2009_07