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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425770Generated: October 31, 2026

1-Aminopiperidine → HCID 11548208, compound

https://huagongshe.com/reaction/425770

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AminopiperidineHCID 16658—
ReactantHCID 11604687HCID 11604687—
ProductHCID 11548208HCID 1154820842%

Reaction Steps

The same procedure described in the preparations a) and b) of Example 3.1. was used to react the 7-bromo-1-(2′,4′-dichlorophenyl)-4,5-dihydro-1H-thieno[2,3-g] indazol-3-carboxylic acid prepared in the Example 2.2 with 1-aminopiperidine. The purification by flash chromatography (oil ether/ethyl acetate 6/4) has given the compound N-piperidinyl-7-bromo-1-(2′,4′-dichlorophenyl)-4,5-dihydro-1H-thieno[2,3-g]indazol-3-carboxamide as white solid with a 42% yield. Rf=0.33 (oil ether/ethyl acetate 6/4); m.p.: 145° C.;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106218B2
Source datasetuspto-grants-2012_01
ORD IDord-50fc174acdde4124b4418f1c053fad6f
Source noteuspto-grants-2012_01