HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Aminopiperidine → HCID 11548208, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Aminopiperidine | HCID 16658 | — |
| Reactant | HCID 11604687 | HCID 11604687 | — |
| Product | HCID 11548208 | HCID 11548208 | 42% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08106218B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-50fc174acdde4124b4418f1c053fad6f |
| Source note | uspto-grants-2012_01 |