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1,1'-Carbonyldiimidazole → HCID 53633805、化合物

HRID 974775
ノート
印刷プレビュー

反応式

HRID 974775 の反応式
[C:1]([N:8]1[CH2:14][CH2:13][CH2:12][C@H:9]1[CH2:10][OH:11])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[C:15](N1C=CN=C1)(N1C=CN=C1)=[O:16].[N:27]1([C:32]2[N:37]=[C:36]([N:38]3[CH2:43][CH2:42][NH:41][CH2:40][CH2:39]3)[CH:35]=[C:34]([N:44]3[CH2:48][CH2:47][CH2:46][CH2:45]3)[N:33]=2)[CH2:31][CH2:30][CH2:29][CH2:28]1.P([O-])(O)(O)=O.[Na+]>C1COCC1>[C:4]([O:3][C:1]([N:8]1[CH2:14][CH2:13][CH2:12][CH:9]1[CH2:10][O:11][C:15]([N:41]1[CH2:42][CH2:43][N:38]([C:36]2[CH:35]=[C:34]([N:44]3[CH2:45][CH2:46][CH2:47][CH2:48]3)[N:33]=[C:32]([N:27]3[CH2:31][CH2:30][CH2:29][CH2:28]3)[N:37]=2)[CH2:39][CH2:40]1)=[O:16])=[O:2])([CH3:7])([CH3:6])[CH3:5]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 682631,1'-CarbonyldiimidazoleHCID 643448(S)-(-)-N-Boc-prolinolHCID 145852434-(Piperazin-1-yl)-2,6-di(pyrrolidin-1-yl)pyrimidineHCID 23672064Monosodium phosphate

生成物 1

HCID 53633805HCID 53633805、化合物収率 69.8%

試薬・触媒・溶媒 1

HCID 8028
Tetrahydrofuran
溶媒

実験手順

A solution of 3 g of BOC-(L)-prolinol in 100 ml of anhydrous THF, cooled at 0° C. with water/ice, under stirring and inert gas atmosphere, is added with 2.9 g of carbonyldiimidazole in portions, then the reaction mixture is warmed to room temperature and stirring is continued for 3 hours. Said solution is added with 4.5 g of N-[2,6-bis(pyrrolidin-1-yl)pyrimidin-4-yl]piperazine in portions and stirring is continued for 18 hours. The reaction mixture is added with 400 ml of an aqueous saturated solution of sodium dihydrogen phosphate and extracted with ethyl acetate (3×100 ml). The combined organic extracts are dried over sodium sulfate and the solvent is evaporated off under reduced pressure. The residue (7.5 g) is purified by silica gel chromatography (eluent hexane/ethyl acetate 7:3), to obtain 5.5 g of (-)-N'-[(1-(tertbutoxycarbonyl) pyrrolidin-2-yl) methyloxycarbonyl]-N-[2,6-bis(pyrrolidin -1-yl)pyrimidin -4 -yl]piperazine, m.p. 147° C., [(α]D-32'(c=0.25 in EtOH).

後処理

  1. stirringstirring
  2. stirringstirring
  3. waitis continued for 18 hours
  4. extractionextracted with ethyl acetate (3×100 ml)
  5. dry with materialThe combined organic extracts are dried over sodium sulfate
  6. customthe solvent is evaporated off under reduced pressure
  7. customThe residue (7.5 g) is purified by silica gel chromatography (eluent hexane/ethyl acetate 7:3)

出典と根拠

ORDレコード
ord-88e3e0aed66c403d849bbae06b643840
出典データセット
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05607930

反応ノート

読み込み中…

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