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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420079Generated: October 29, 2026

(1R,2S)-ethyl 1-((2S,4S)-4-(8-chloro-7-methoxy-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)quinolin-4-yloxy)-2-(hex-5-enyl(methyl)carbamoyl)pyrrolidine-1-carboxamido)-2-vinylcyclopropanecarboxylate → (1R,2S)-1-((2S,4S)-4-(8-chloro-7-methoxy-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)quinolin-4-yloxy)-2-(hex-5-enyl(methyl)carbamoyl)pyrrolidine-1-carboxamido)-2-vinylcyclopropanecarboxylic acid

https://huagongshe.com/reaction/420079

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(1R,2S)-ethyl 1-((2S,4S)-4-(8-chloro-7-methoxy-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)quinolin-4-yloxy)-2-(hex-5-enyl(methyl)carbamoyl)pyrrolidine-1-carboxamido)-2-vinylcyclopropanecarboxylateHCID 57816697—
ReactantOctadec-7-ene-4-carboxylic acidHCID 73991637—
Product(1R,2S)-1-((2S,4S)-4-(8-chloro-7-methoxy-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)quinolin-4-yloxy)-2-(hex-5-enyl(methyl)carbamoyl)pyrrolidine-1-carboxamido)-2-vinylcyclopropanecarboxylic acidHCID 5781666460%

Reaction Steps

Compound 117 was synthesized from compound 116 as a white solid in 60% yield, following the procedure as described for compound 55c.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093379B2
Source datasetuspto-grants-2012_01
ORD IDord-0ce9f00638f546999734a29254afd7f2
Source noteuspto-grants-2012_01