HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1667712Generated: October 31, 2026
1-Methylpiperazine → HCID 86642821, compound
https://huagongshe.com/reaction/1667712
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 86642820 | HCID 86642820 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86642821 | HCID 86642821 | 37.6% |
Reaction Steps
To a mixture of 0.10 g (0.24 mmole) of 4-(4-chloro-phenyl)-2-(4-formyl-2-nitro-phenylamino)-thiazole-5-carboxylic acid amide (VI.18a), 0.31 g (1.44 mmole) of sodium triacetoxyborohydride and 5 mL of dichloromethane was added 0.04 mL (0.36 mmole) of 1-methylpiperazine. The mixture was stirred at room temperature for 4 hours and then diluted with dichloromethane, washed with aqueous saturated sodium bicarbonate solution, brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography, eluting with methanol-dichloromethane (gradient 0:100-15:85) to give 0.044 g of 4-(4-chloro-phenyl)-2-[4-(4-methyl-piperazin-1-ylmethyl)-2-nitro-phenylamino]-thiazole-5-carboxylic acid amide (VI.18b).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08044213B2 |
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| Source dataset | uspto-grants-2011_10 |
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| ORD ID | ord-06b958753f244eb683fae3e0f4c9f2b8 |
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| Source note | uspto-grants-2011_10 |
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