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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1717702Generated: November 3, 2026

1,2-Dichloroethane → HCID 178450645, compound

https://huagongshe.com/reaction/1717702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Isopropylphenylacetic acidHCID 78230—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178450643HCID 178450643—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178450645HCID 178450645—

Reaction Steps

To a solution of enantiomer A of butyl 1-[(trans-4-tert-butylcyclohexyl)amino]indane-5-carboxylate, (41 mg, 0.11 mmol) in CH2CL2 (3 mL) was added (4-isopropylphenyl)acetic acid (98 mg, 0.55 mmol), EDC (105 mg, 0.55 mmol), HOBt (74 mg, 0.55 mmol) and DIEA (200 μL, 1.10 mmol). After stirring at room temperature for 18 h, the reaction mixture was poured into saturated aqueous NaHCO3 (10 mL) and extracted with EtOAc (20 mL). The organic layer was washed with brine (2×10 mL), dried over Na2SO4, filtered and concentrated. Chromatography (10% EtOAc in Hexane) gave butyl 1-{(trans-4-tert-butylcyclohexyl)[(4-isopropylphenyl)acetyl]amino}indane-5-carboxylate. HPLC/MS: m/z=532.3 (M+1), Rt=3.15 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803951B2
Source datasetuspto-grants-2010_09
ORD IDord-75b336d0194541c7a6a5c415d8ff13ee
Source noteuspto-grants-2010_09