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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541665Generated: October 31, 2026

4-Carboxy-1,2,3-triazole → HCID 178520319, compound

https://huagongshe.com/reaction/541665

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Carboxy-1,2,3-triazoleHCID 140120—
ReactantN-[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]-2-piperidin-4-ylacetamide tris(trifluoroacetate)HCID 86636131—
ProductHCID 178520319HCID 17852031948%

Reaction Steps

The desired compound was prepared according to the procedure of Example A27 using N-[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]-2-piperidin-4-ylacetamide tris(trifluoroacetate) and 2H-1,2,3-triazole-4-carboxylic acid as starting materials in 48% yield. 1H NMR (300 MHz, DMSO-d6): δ 10.12 (s, 1H), 9.41 (m, 2H), 9.15 (s, 1H), 8.32 (m, 2H), 8.21 (m, 2H), 7.65 (s, 1H), 7.30 (d, 1H), 7.05 (d, 1H), 4.52 (m, 2H), 3.19 (m, 2H), 2.99 (m, 4H), 2.32 (m, 2H), 2.12 (m, 1H), 1.80 (m, 2H), 1.20 (m, 2H). LCMS for C27H28ClN10O2 (M+H)+: m/z=559.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871753B2
Source datasetuspto-grants-2014_10
ORD IDord-1470416d98dd4b31a50c4256cde82dee
Source noteuspto-grants-2014_10