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2,5-Dihydroxybenzoic acid → HCID 11508769、化合物

HRID 2373327
ノート
印刷プレビュー

反応式

HRID 2373327 の反応式
[OH:1][C:2]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12][NH:13][C@H:14]([CH2:16]/[CH:17]=[CH:18]/[C:19]1[CH:20]=[N:21][CH:22]=[C:23]([O:25][CH3:26])[CH:24]=1)[CH3:15].C(OCC)(=O)C>C(O)C>[OH:1][C:2]1[CH:10]=[CH:9][C:8]([OH:11])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH3:12][NH:13][C@H:14]([CH2:16]/[CH:17]=[CH:18]/[C:19]1[CH:20]=[N:21][CH:22]=[C:23]([O:25][CH3:26])[CH:24]=1)[CH3:15]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 34692,5-Dihydroxybenzoic acidHCID 8857Ethyl AcetateHCID 102624065-(5-Methoxy-3-pyridinyl)-N-methyl-4-penten-2-amine, (2S,4E)-

生成物 1

HCID 11508769HCID 11508769、化合物収率 91%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒3 回

実験手順

A hot solution of 2,5-dihydroxybenzoic acid (gentisic acid) (0.582 g, 3.78 mmol) in absolute ethanol (1 mL) was added to a warm solution of (2S)-(4E)-N-methyl-5-(5-methoxy-3-pyridinyl)-4-penten-2-amine (1.00 g, 4.85 mmol, 86.7% E isomer by GC-FID) in absolute ethanol (1 mL), using additional ethanol (2 mL) in the transfer. The resulting mixture was concentrated via rotary evaporation, leaving 1.5 mL of ethanol in the solution. With stirring and heating to near reflux, crystallization occurred. The resulting hot mixture was treated drop-wise with ethyl acetate (5.5 mL). After cooling to room temperature, the mixture was further cooled at 5° C. for 48 h. The resulting solids were filtered, washed with ethyl acetate (2×5 mL) and dried at 50° C. to give 1.24 g (91%) of an off-white powder (98.0% E isomer by GC-FID for the free base). To remove the color from the sample, the material was recrystallized from ethanol/isopropanol (3.5 mL:5.5 mL) to give 1.03 g (83% recovery) of an off-white powder and subsequently recrystallized from ethanol/ethyl acetate (3 mL:12 mL) to give 0.90 g (87% recovery) of a white, crystalline powder, mp 166-167° C.

後処理

  1. concentrationThe resulting mixture was concentrated via rotary evaporation
  2. customleaving 1.5 mL of ethanol in the solution
  3. temperatureheating to near reflux, crystallization
  4. temperaturethe mixture was further cooled at 5° C. for 48 h
  5. filtrationThe resulting solids were filtered
  6. washwashed with ethyl acetate (2×5 mL)
  7. customdried at 50° C.

出典と根拠

ORDレコード
ord-dacd4a9efac8448199f58c9bb7281bdc
出典データセット
uspto-grants-2008_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07459469B2

反応ノート

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