HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485874Generated: October 30, 2026
HCID 59242670, compound → HCID 59242651, compound
https://huagongshe.com/reaction/1485874
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 59242670 | HCID 59242670 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59242651 | HCID 59242651 | — |
Reaction Steps
To a solution of 4-[5-(5-chloro-thiophen-2-yl)-6-trifluoromethyl-pyridazin-3-yl]-piperazine-1-carboxylic acid tert-butyl ester (D15) (0.114 g, 0.25 mmol) in methanol (10 ml) was added Amberlyst® 15 ion exchange resin, acidic form (4.1 mmol/g) (0.305 g, 1.25 mmol) and the reaction mixture was shaken at room temperature for 18 h. After this period, the mixture was filtered and then a saturated solution of ammonia in methanol was added. The mixture was shaken for 1 h, filtered and the filtrate evaporated in vacuo. The residue was then purified by column chromatography (silica gel; 3% ammonia in methanol (7M)/dichloromethane). The desired fractions were collected and evaporated in vacuo. The crude product was dissolved in a 2 M solution of hydrochoric acid in diethyl ether and the mixture stirred at room temperature for 16. The solvent was evaporated in vacuo. The solid obtained was triturated from diethyl ether to yield E27 (0.062 g, 87%). C13H12ClF3N4S requires 348; Found 349 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422296B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-f32c5ef934484969b864ed950d1e88d6 |
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| Source note | uspto-grants-2016_08 |
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