1,1-Dimethylethyl (3S)-4-[(4-chlorophenyl)sulfonyl]-3-methyl-1-piperazinecarboxylate → (2S)-1-[(4-Chlorophenyl)sulfonyl]-2-methylpiperazine hydrochloride

HRID 41294

反応式

HRID 41294 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([N:11]2[CH2:16][CH2:15][N:14](C(OC(C)(C)C)=O)[CH2:13][C@@H:12]2[CH3:24])(=[O:10])=[O:9])=[CH:4][CH:3]=1>Cl.O1CCOCC1>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:8]([N:11]2[CH2:16][CH2:15][NH:14][CH2:13][C@@H:12]2[CH3:24])(=[O:9])=[O:10])=[CH:6][CH:7]=1

参加物

4

反応物 1

HCID 582844531,1-Dimethylethyl (3S)-4-[(4-chlorophenyl)sulfonyl]-3-methyl-1-piperazinecarboxylate

生成物 1

HCID 67028562(2S)-1-[(4-Chlorophenyl)sulfonyl]-2-methylpiperazine hydrochloride

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒HCID 312751,4-Dioxane溶媒

実験手順

1,1-Dimethylethyl (3S)-4-[(4-chlorophenyl)sulfonyl]-3-methyl-1-piperazinecarboxylate (may be prepared as described in Description 3) (crude weight 24.14 g, theoretical 49.9 mmol) was suspended in 4M HCl in 1,4-dioxane (80 mL, excess) and stirred vigorously for 3 hours. The sample was evaporated, suspended in diethyl ether (100 mL) and filtered through a sinter. The collected solid was dried under vacuum at 40° C. for 18 hours to yield the title compound as a yellow solid (15.45 g).

後処理

  1. customThe sample was evaporated
  2. filtrationfiltered through a sinter
  3. customThe collected solid was dried under vacuum at 40° C. for 18 hours

出典と根拠

ORDレコード
ord-a1987813c1de433c9b0312165c51819f
出典データセット
uspto-grants-2013_09
特許番号
US08530478B2

関連ノート

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