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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420076Generated: October 29, 2026

N-methylhex-5-en-1-amine 4-methylbenzenesulfonate → (2S,4S)-tert-butyl 4-(8-chloro-7-methoxy-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)quinolin-4-yloxy)-2-(hex-5-enyl(methyl)carbamoyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/420076

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methylhex-5-en-1-amine 4-methylbenzenesulfonateHCID 46737741—
Reactant(2S,4R)-tert-butyl 2-(N-(hex-5-enyl)-N-methyl-carbamoyl)-4-hydroxypyrrolidine-1-carboxylateHCID 57816706—
Reactant(2S,4S)-1-(tert-butoxycarbonyl)-4-(8-chloro-7-methoxy-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)quinolin-4-yloxy)pyrrolidine-2-carboxylic acidHCID 57816711—
Product(2S,4S)-tert-butyl 4-(8-chloro-7-methoxy-2-(3-(trifluoromethyl)-1H-pyrazol-1-yl)quinolin-4-yloxy)-2-(hex-5-enyl(methyl)carbamoyl)pyrrolidine-1-carboxylateHCID 5781670087%

Reaction Steps

Compound 114 was synthesized from compounds 32a and 113 as white foam in 87% yield, following the procedure as described for compound 48.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093379B2
Source datasetuspto-grants-2012_01
ORD IDord-f4c9ea4e95d14be785a6da29a6dfddbe
Source noteuspto-grants-2012_01