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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639635Generated: October 28, 2026

1,2-Dichloroethane → HCID 178452920, compound

https://huagongshe.com/reaction/1639635

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-(Morpholinomethyl)benzene-1,2-diamineHCID 25193309—
ReactantHCID 178452921HCID 178452921—
SolventDimethylformamideHCID 6228—
ProductHCID 178452920HCID 17845292096%

Reaction Steps

A mixture of 4-tert-butoxycarbonylamino-1H-pyrazole-3-carboxylic acid (10.0 g, 44.1 mmol), 4-morpholin-4-ylmethyl-benzene-1,2-diamine (10.0 g, 48.5 mmol), EDC (10.14 g, 52.9 mmol) and HOBt (7.15 g, 52.9 mmol) in DMF (150 mL) was stirred at ambient temperature for 20 h and then the majority of the solvent removed in vacuo. The residue was partitioned between EtOAc (150 mL) and saturated aqueous NaHCO3 (150 mL), the layers separated and the organic portion washed with brine, dried over MgSO4 and reduced in vacuo to give [3-(2-amino-4-morpholin-4-ylmethyl-phenylcarbamoyl)-1H-pyrazol-4-yl]-carbamic acid tert-butyl ester (17.6 g, 96%) as a brown solid. LC/MS analysis indicates product contains 15% of the di-amide. This shows at approx. 5% level in 1H NMR. Di-amide is cleaved in subsequent step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110573B2
Source datasetuspto-grants-2012_02
ORD IDord-701e895c8dd54581ad0b6bd67d5e748a
Source noteuspto-grants-2012_02