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1-Methylpiperazine → 5-{4-[(4-Methylpiperazin-1-yl)methyl]benzamido}-2-(naphthalen-2-ylamino)thiazole-4-carboxamide

HRID 512532
ノート
印刷プレビュー

反応式

HRID 512532 の反応式
[NH2:1][C:2]1[S:6][C:5]([NH:7][C:8]2[CH:17]=[CH:16][C:15]3[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=3)[CH:9]=2)=[N:4][C:3]=1[C:18]([NH2:20])=[O:19].C(N(CC)C(C)C)(C)C.Cl[CH2:31][C:32]1[CH:40]=[CH:39][C:35]([C:36](Cl)=[O:37])=[CH:34][CH:33]=1.[CH3:41][N:42]1[CH2:47][CH2:46][NH:45][CH2:44][CH2:43]1>CC(N(C)C)=O.C(OCC)(=O)C>[CH3:41][N:42]1[CH2:47][CH2:46][N:45]([CH2:31][C:32]2[CH:40]=[CH:39][C:35]([C:36]([NH:1][C:2]3[S:6][C:5]([NH:7][C:8]4[CH:17]=[CH:16][C:15]5[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=5)[CH:9]=4)=[N:4][C:3]=3[C:18]([NH2:20])=[O:19])=[O:37])=[CH:34][CH:33]=2)[CH2:44][CH2:43]1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 531671-MethylpiperazineHCID 701364-(Chloromethyl)benzoyl chlorideHCID 81531DiisopropylethylamineHCID 867033695-Amino-2-(naphthalen-2-ylamino)thiazole-4-carboxamide

生成物 1

HCID 725508545-{4-[(4-Methylpiperazin-1-yl)methyl]benzamido}-2-(naphthalen-2-ylamino)thiazole-4-carboxamide収率 11%

試薬・触媒・溶媒 2

HCID 8857Ethyl Acetate溶媒
HCID 31374Dimethylacetamide溶媒2 回

実験手順

To a mixture of 5-amino-2-(naphthalen-2-ylamino)thiazole-4-carboxamide (0.50 g, 1.76 mmol) and. N,N-diisopropylethylamine (0.3 mL, 1.94 mmol) in DMA (30 mL) was added 4-chloromethylbenzoyl chloride (0.37g, 1.94 mmol) at 0° C. The mixture was stirred for 3 hrs at rt. Then 1-methylpiperazine (0.1 mL, 0.95 mmol) was added to the mixture (0.083 g in 5 mL DMA), and the mixture was stirred for 16 hrs at rt. The reaction mixture was diluted with ethyl acetate (150 mL), washed with water, and dried over Na2SO4. The solvent was evaporated under reduced pressure, and the crude residue was purified by silica gel column chromatograph eluted with 5% MeOH in DCM to give 0.010 g (11% yield) of the titled compound.

後処理

  1. stirringthe mixture was stirred for 16 hrs at rt
  2. washwashed with water
  3. dry with materialdried over Na2SO4
  4. customThe solvent was evaporated under reduced pressure
  5. customthe crude residue was purified by silica gel column chromatograph
  6. washeluted with 5% MeOH in DCM

出典と根拠

ORDレコード
ord-954b9c94b4784ce980d33420695ee65d
出典データセット
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09102637B2

反応ノート

読み込み中…

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