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HRID 469130作成日:2026年10月26日

1-(1-Methyl-4-piperidinyl)piperazine → Ammonia

https://huagongshe.com/reaction/469130

反応式

関与物質

役割名称HCID仕込み量
反応物1-(1-Methyl-4-piperidinyl)piperazineHCID 566324—
反応物TrimethylaluminumHCID 16682925—
反応物ethyl 5-({Cyclopropyl[(4-methoxy-2,6-dimethylphenyl)sulfonyl]amino}methyl)-1,3,4-thiadiazole-2-carboxylateHCID 58393201—
溶媒1,2-DichloroethaneHCID 11—
生成物AmmoniaHCID 222—
生成物N-Cyclopropyl-4-methoxy-2,6-dimethyl-N-[(5-{[4-(1-methylpiperidin-4-yl)piperazin-1-yl]carbonyl}-1,3,4-thiadiazol-2-yl)methyl]benzenesulfonamideHCID 58393376—

反応手順

The title compound was prepared according to general procedure AT using ethyl 5-({cyclopropyl[(4-methoxy-2,6-dimethylphenyl)sulfonyl]amino}methyl)-1,3,4-thiadiazole-2-carboxylate (30 mg, 0.07 mmol), 1-(1-methylpiperidin-4-yl)piperazine (26 mg, 0.14 mmol) and trimethylaluminium (2 M in toluene, 0.07 mL) in DCE (5 mL). The crude product was purified using FCC, eluting with 95:4.5:0.5 DCM:MeOH:NH3, to afford the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08623859B2
出典データセットuspto-grants-2014_01
ORD IDord-79758d6df2224fe7b3180851d14d23a5
出典メモuspto-grants-2014_01