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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1428239Generated: October 30, 2026

1,2-Dichloroethane → HCID 58014781, compound

https://huagongshe.com/reaction/1428239

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
ReactantAmmoniaHCID 222—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 58014948HCID 58014948—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 58014781HCID 5801478191.8%

Reaction Steps

To a solution of 4-((1-(tert-butoxycarbonyl)piperidin-4-yl)methylamino)-2-chloropyrimidine-5-carboxylic acid (0.353 g, 0.953 mmol) and HOBt (0.219 g, 1.43 mmol) in DMF (5 mL), EDC (0.274 g, 1.43 mmol) was added. After being stirred for 1 h, NH3 (0.5 M in dioxane, 5.5 mL, 2.75 mmol) was added. The mixture was stirred for 20 h. Water and EtOAc were added. The organic phase was separated, washed with 1N HCl, then with 5% NaHCO3, dried over Na2SO4, concentrated in vacuo to give tert-butyl 4-((2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-5-carbamoylpyrimidin-4-ylamino)methyl)piperidine-1-carboxylate as a solid (0.410 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937070B2
Source datasetuspto-grants-2015_01
ORD IDord-e546b2f7cb0c4926a74e8c75f21fa312
Source noteuspto-grants-2015_01