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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510181Generated: November 1, 2026

1,2-Dichloroethane → HCID 89495512, compound

https://huagongshe.com/reaction/510181

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 89486952HCID 89486952—
SolventDimethylformamideHCID 6228—
ProductHCID 89495512HCID 89495512110.4%

Reaction Steps

To a mixture of 2-[(5-bromopyridin-3-yl)amino]-2-methylpropanoic acid I-4b (2.0 g, 7.72 mmol), 2,2,2-trifluoroethylamine (1.214 mL, 15.44 mmol), HOBT (1.773 g, 11.58 mmol) and DIPEA (2.70 mL, 15.44 mmol) in DMF (20 mL) was added EDC (2.220 g, 11.58 mmol). The mixture was allowed to stir at RT for 18 hr. The reaction was quenched into water (100 mL) and ethyl acetate (100 mL) and aq. KHSO4 added to adjust the pH to 6.5. Organic layer removed, washed with aqueous NaHCO3 (50 mL) and then brine (50 mL). The aqueous extracts were washed with ethyl acetate (50 mL). Organics combined, dried over sodium sulfate, filtered thru a pad of silica and concentrated to give a solid 2.9 gms. Solid slurried in ether, sonicated and filtered to give 2.4 g, (91%) title compound, I-4, as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096598B2
Source datasetuspto-grants-2015_08
ORD IDord-ae03335f36964041b009c830739f6c0f
Source noteuspto-grants-2015_08