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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366545Generated: October 30, 2026

1,2-Dichloroethane → HCID 87210495, compound

https://huagongshe.com/reaction/1366545

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant4-MethylmorpholineHCID 7972—
ReactantHOAtHCID 181649—
Reactant(R)-3-(Benzyloxy-formyl-amino)-2-cyclopentylmethyl-propionic acidHCID 21305218—
ReactantHCID 87210185HCID 87210185—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 87210495HCID 8721049592%

Reaction Steps

To a solution of racemic 1-(2-chloro-5-fluoro-6-hydrazino-4-pyrimidinyl)-N,N,4,4-tetramethyl-3-pyrrolidinamine (7.37 g, 24.34 mmol, prepared according to the procedures of Example 133) in DMF (77 mL) was added (2R)-3-cyclopentyl-2-({formyl[(phenylmethyl)oxy]amino}methyl)propanoic acid (7.08 g, 23.18 mmol), N-methylmorpholine (12.75 mL, 116.0 mmol), 1-hydroxy-7-azabenzotriazole (3.79 g, 27.85 mmol), and EDC (5.33 g, 27.80 mmol). The solution was stirred overnight and was then diluted with Et2O (100 mL) and washed with water (3×100 mL). The combined aqueous phase was extracted with a fresh portion of Et2O (100 mL), and this organic phase was washed with a fresh portion of water (50 mL). The combined organic phase was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo. The residue was diluted with EtOAc (200 mL), and the resulting solution was dried over anhydrous Na2SO4, filtered, and concentrated in vacuo to afford crude [(2R)-3-(2-{2-chloro-6-[4-(dimethylamino)-3,3-dimethyl-1-pyrrolidinyl]-5-fluoro-4-pyrimidinyl}hydrazino)-2-(cyclopentylmethyl)-3-oxopropyl][(phenylmethyl)oxy]formamide (12.52 g, 92% yield, mixture of diastereomers). LCMS: (M+H)+: 590.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893056B2
Source datasetuspto-grants-2011_02
ORD IDord-1c64d3c640b94ab59d381b16d99615d6
Source noteuspto-grants-2011_02