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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 226442Generated: October 27, 2026

Triethylamine → HCID 86603747, compound

https://huagongshe.com/reaction/226442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMagnesium BromideHCID 82241—
ReactantEthyl (dimethoxyphosphoryl)(fluoro)acetateHCID 12696184—
Reactant6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloronicotinaldehydeHCID 86603748—
SolventTetrahydrofuranHCID 8028—
SolventWater ethylacetateHCID 22728543—
ProductHCID 86603747HCID 8660374781.6%

Reaction Conditions

Temperature7.5 °C

Reaction Steps

To a mixture of ethyl (dimethoxyphosphoryl)(fluoro)acetate (1.46 g) and magnesium bromide (1.33 g) in THF (20 ml) was added dropwise to a Et3N (0.92 ml) with stirring at 0-15° C. under atmospheric pressure of nitrogen, and the reaction mixture was stirred at same condition for an hour. A solution of 6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloronicotinaldehyde (1.36 g) in THF (10 ml) solution was added the above mixture and resultant mixture was stirred at 0-15° C. for 4 hours. The reaction mixture was poured into a mixture of AcOEt-H2O and the organic layer was washed with brine and dried over MgSO4— The solvent was evaporated in vacuo and the residue was chromatographed on silicagel eluting with AcOEt-n-hexane (3:7). The eluted fractions containing the desired product were collected and evaporated in vacuo to give ethyl (2Z)-3-(6-{[(3R)-1-benzyl-3-pyrrolidinyl]amino}-5-chloro-3-pyridinyl)-2-fluoroacrylate (1.42 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07557127B2
Source datasetuspto-grants-2009_07
ORD IDord-6fcebd23b8294e7dbcbcb0151c07f74e
Source noteuspto-grants-2009_07