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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542011Generated: October 25, 2026

3-Isocyanatothiophene → 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-3-thienylpiperidine-1-carboxamide bis(trifluoroacetate)

https://huagongshe.com/reaction/542011

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-IsocyanatothiopheneHCID 2776380—
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-3-thienylpiperidine-1-carboxamide bis(trifluoroacetate)HCID 8663635130%

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-isocyanatothiophene as the starting materials in 30% yield. LCMS for C29H31ClN7O2S (M+H)+: m/z=576.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-fa5908a42087477ea30ae467e96dad6d
Source noteuspto-grants-2014_10