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Hydrochloric Acid → Ammonia

HRID 2383365
ノート
印刷プレビュー

反応式

HRID 2383365 の反応式
C(OC([N:8]([CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][N:25]1[CH2:30][CH2:29][CH:28]([CH2:31][N:32]2[CH:36]=[N:35][C:34]([C@:37]([CH:45]3[CH2:50][CH2:49][CH2:48][CH2:47][CH2:46]3)([OH:44])[C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)=[N:33]2)[CH2:27][CH2:26]1)C(OC(C)(C)C)=O)=O)(C)(C)C.Cl.C(OCC)C>ClCCl>[NH3:8].[NH2:8][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][N:25]1[CH2:26][CH2:27][CH:28]([CH2:31][N:32]2[CH:36]=[N:35][C:34]([C@@:37]([CH:45]3[CH2:46][CH2:47][CH2:48][CH2:49][CH2:50]3)([C:38]3[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=3)[OH:44])=[N:33]2)[CH2:29][CH2:30]1
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 3

HCID 313Hydrochloric AcidHCID 3283Diethyl EtherHCID 59145968Di-tert-butyl{9-[4-({3-[(R)-cyclohexyl(hydroxy)phenylmethyl]-1H-1,2,4-triazol-1-yl}methyl)piperdin-1-yl]nonyl}imidodicarbonate

生成物 2

HCID 222AmmoniaHCID 59145972(R)-(1-{[1-(9-aminononyl)piperidin-4-yl]methyl}-1H-1,2,4-triazol-3-yl)(cyclohexyl) phenylmethanol

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

Di-tert-butyl{9-[4-({3-[(R)-cyclohexyl(hydroxy)phenylmethyl]-1H-1,2,4-triazol-1-yl}methyl)piperdin-1-yl]nonyl}imidodicarbonate (Preparation 5, 2.6 g, 3.7 mmol) was dissolved in dichloromethane (15 ml) and hydrogen chloride in diethylether (2M, 15 ml, 30 mmol) added. After stirring at room temperature for 5 hours the solvent was removed in vacuo, the residue was partitioned between dichloromethane (200 ml) and saturated aqueous sodium bicarbonate solution (200 ml). The organic layer was separated, dried over magnesium sulphate, filtered and the solvent removed in vacuo. The residue was purified by column chromatography on silica gel eluting with dichloromethane:methanol:880 ammonia (97.5:2.5:0.25, by volume) to furnish the title compound as a clear oil, in 70% yield, 1.29 g (contains 10% of other triazole regio-isomer).

後処理

  1. customwas removed in vacuo
  2. customthe residue was partitioned between dichloromethane (200 ml) and saturated aqueous sodium bicarbonate solution (200 ml)
  3. customThe organic layer was separated
  4. dry with materialdried over magnesium sulphate
  5. filtrationfiltered
  6. customthe solvent removed in vacuo
  7. customThe residue was purified by column chromatography on silica gel eluting with dichloromethane

出典と根拠

ORDレコード
ord-38e3ba30746a47c5b598f07b623da761
出典データセット
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08263623B2

反応ノート

読み込み中…

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