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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020102Generated: October 29, 2026

1,2-Dichloroethane → 1253955-17-7

https://huagongshe.com/reaction/1020102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant2,4-Dimethylbenzoic acidHCID 11897—
ReactantHCID 59563703HCID 59563703—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Product1253955-17-7HCID 59563805—

Reaction Steps

To 2,4-dimethylbenzoic acid in pyridine was added EDC, DMAP, and tert-butyl 2-(4-(hydroxymethyl)phenyl)-3-(isoquinolin-6-ylamino)-3-oxopropylcarbamate (E139), and the solution was capped and stirred overnight. The mixture was poured into EtOAc/NaHCO3(sat) and the aqueous layer was further extracted with EtOAc. The organics were dried (MgSO4), filtered, and evaporated. Column chromatography (SiO2, 0-5% MeOH/CH2Cl2 gradient) gave pure 4-(3-(tert-butoxycarbonylamino)-1-(isoquinolin-6-ylamino)-1-oxopropan-2-yl)benzyl 2,4-dimethylbenzoate (E145).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716310B2
Source datasetuspto-grants-2014_05
ORD IDord-1e46df8d9356423e9f4a1e469fcd1827
Source noteuspto-grants-2014_05