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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1822445Generated: November 1, 2026

Cyclohexanemethylamine → (1R,2S)-1 {[(2S,4R)-1-[(1S)-1-(Cyclohexylmethyl-carbamoyl)-2-phenyl-ethylcarbamoyl]4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}-2-vinyl-cyclopropanecarboxylic acid

https://huagongshe.com/reaction/1822445

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanemethylamineHCID 76688—
ReactantL-Phenylalanine, N-[(1,1-dimethylethoxy)carbonyl]-HCID 77857—
Reactant2-{[(Tert-butoxy)carbonyl]amino}-3,3-dimethylbutanoic acidHCID 5046859—
ReactantChlorocarbamateHCID 22035886—
Reactant[1-(2-Hydroxy-indan-1-ylcarbamoyl)-2,2-dimethyl-propyl]-carbamic acid tert.butyl esterHCID 68488177—
Reactant1-{[1-[1-(2-Hydroxy-indan-1-ylcarbamoyl)-2,2-dimethyl-propylcarbamoyl]-4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}-2-vinyl-cyclopropanecarboxylic acid ethyl esterHCID 68491628—
Product(1R,2S)-1 {[(2S,4R)-1-[(1S)-1-(Cyclohexylmethyl-carbamoyl)-2-phenyl-ethylcarbamoyl]4-(7-methoxy-2-phenyl-quinolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}-2-vinyl-cyclopropanecarboxylic acidHCID 68488115—

Reaction Steps

N-(tert-butoxycarbonyl)-L-phenylalanine was attached to the resin as described for the preparation of compound 16 followed by reaction with cyclohexanemethylamine as described for the preparation of 17 and removal of the Boc group as described for 18. The afforded compound was then reacted with the chlorocarbamate achieved from 12 as described for the preparation of 13 which gave the title compound. Purity by HPLC>95%. M+H+760.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07608590B2
Source datasetuspto-grants-2009_10
ORD IDord-e05eed28e35247ca8f3ef57c59c64229
Source noteuspto-grants-2009_10