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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878747Generated: October 28, 2026

Pyrrolidine → HCID 68290211, compound

https://huagongshe.com/reaction/878747

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 86707383HCID 86707383—
SolventTolueneHCID 1140—
ProductHCID 68290211HCID 6829021124.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of ethyl 4-({(1-bromo-4-methylisoquinolin-3-yl)[4-(trifluoromethoxy)-benzyl]amino}sulfonyl)benzoate (93.5 mg, 0.15 mmol) prepared in Example 9-(1), pyrrolidine (0.015 mL, 0.18 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (9.3 mg, 0.015 mmol), trisdibenzylideneacetone dipalladium (6.9 mg, 0.0075 mmol) and sodium-t-butoxide (20.2 mg, 0.21 mmol) in toluene (2 mL) was stirred at 100° C. for 4 hours under argon atmosphere. The mixture was cooled to room temperature, and then filtered, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane=10%→25%) to give ethyl 4-({(4-methyl-1-pyrrolidin-1-ylisoquinolin-3-yl) [4-(trifluoromethoxy)benzyl]amino}sulfonyl)benzoate (22.4 mg, 24%) as a yellow viscous material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987445B2
Source datasetuspto-grants-2015_03
ORD IDord-c5eeb46deffa412380fd2df6c8d18be3
Source noteuspto-grants-2015_03