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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542009Generated: October 25, 2026

3-Isocyanato-2-methylfuran → 4-(2-{[6-Chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]oxy}ethyl)-N-(2-methyl-3-furyl)piperidine-1-carboxamide bis(trifluoroacetate)

https://huagongshe.com/reaction/542009

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Isocyanato-2-methylfuranHCID 24229546—
Reactant6-Chloro-12-(2-piperidin-4-ylethoxy)-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene tris(trifluoroacetate)HCID 86636347—
Product4-(2-{[6-Chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]oxy}ethyl)-N-(2-methyl-3-furyl)piperidine-1-carboxamide bis(trifluoroacetate)HCID 866363498%

Reaction Steps

The desired compound was prepared according to the procedure of Example D41 using 6-chloro-12-(2-piperidin-4-ylethoxy)-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaene tris(trifluoroacetate) and 3-isocyanato-2-methylfuran as the starting materials in 8% yield. LCMS for C30H33ClN7O3 (M+H)+: m/z=574.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-7a1ad0e49b444cdba6740e655e616550
Source noteuspto-grants-2014_10