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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 542071Generated: October 30, 2026

Methoxyacetyl chloride → 6-Chloro-12-{2-[4-(methoxyacetyl)piperazin-1-yl]-2-oxoethoxy}-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 bis(trifluoroacetate)

https://huagongshe.com/reaction/542071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetyl chlorideHCID 96623—
Reactant6-Chloro-12-(2-oxo-2-piperazin-1-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 86636393—
Product6-Chloro-12-{2-[4-(methoxyacetyl)piperazin-1-yl]-2-oxoethoxy}-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 bis(trifluoroacetate)HCID 8663640077%

Reaction Steps

The desired compound was prepared according to the procedure of Example D94 using 6-chloro-12-(2-oxo-2-piperazin-1-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 methoxyacetyl chloride as the starting materials in 77% yield. LCMS for C26H29ClN7O4 (M+H)+: m/z=538.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-b2788176c10b436abe55490cd81435cf
Source noteuspto-grants-2014_10