Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521137Generated: October 25, 2026

Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) → (cis-2,3,4,4a,9,9a-Hexahydro-indeno[2,1-b]pyridin-1-yl)-(1H-indazol-6-yl)-methanone

https://huagongshe.com/reaction/521137

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactant1H-indazole-6-carboxylic acidHCID 16227938—
Reactantcis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridineHCID 58123900—
Product(cis-2,3,4,4a,9,9a-Hexahydro-indeno[2,1-b]pyridin-1-yl)-(1H-indazol-6-yl)-methanoneHCID 672245715%

Reaction Steps

The title compound is prepared from 1H-indazole-6-carboxylic acid and cis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine following a procedure analogous to that described in Example 1 [2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate is used]. Yield: 5% of theory; LC (method 4): tR=1.92 min; Mass spectrum (ESI+): m/z=318 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328072B2
Source datasetuspto-grants-2016_05
ORD IDord-3d98cf6c9f724d7e8f919572ebdde6f4
Source noteuspto-grants-2016_05