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4-Methoxybenzoic Acid → HCID 10252289、化合物

HRID 567105
ノート
印刷プレビュー

反応式

HRID 567105 の反応式
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=O)=[CH:5][CH:4]=1.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.[F:34][C:35]([F:53])([F:52])[O:36][C:37]1[CH:42]=[CH:41][C:40]([CH:43]2[C:48]3[CH:49]=[CH:50][S:51][C:47]=3[CH2:46][CH2:45][NH:44]2)=[CH:39][CH:38]=1.C(N(CC)C(C)C)(C)C>CN(C)C=O.O>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]([C:7]([N:44]2[CH2:45][CH2:46][C:47]3[S:51][CH:50]=[CH:49][C:48]=3[CH:43]2[C:40]2[CH:39]=[CH:38][C:37]([O:36][C:35]([F:34])([F:53])[F:52])=[CH:42][CH:41]=2)=[O:9])=[CH:10][CH:11]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 74784-Methoxybenzoic AcidHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2777349HCID 2777349、化合物

生成物 1

HCID 10252289HCID 10252289、化合物収率 117%

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide溶媒

実験手順

4-Methoxybenzoic acid (0.64 g, 4.2 mmol) was dissolved in N,N-dimethylformamide (25 ml) and 1-hydroxybenzotriazole (0.71 g, 5 mmol) was added followed by N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.96 g, 5 mmol). The resulting mixture was stirred at room temperature for 30 minutes. 4-(4-Trifluoromethoxyphenyl)-4,5,6,7-tetrahydro-thieno[3,2-c]pyridine (1.5 g, 5 mmol) followed by N,N-diisopropylethylamine (1.4 ml, 8.4 mmol) were added and the resulting mixture was stirred at room temperature for 16 hours. Water (10 ml) was added and the mixture was extracted with diethyl ether (3×20 ml). The combined organic extracts were washed with saturated aqueous ammonium chloride (20 ml), dried over MgSO4 and concentrated in vacuo. The residue was purified by column chromatography over silica gel eluting with a mixture of ethyl acetate and heptane (1:2). The pure fractions were pooled and concentrated in vacuo. The residue was crystallised from a mixture of methyl tert-butyl ether and heptane to afford 2.13 g (98%) of the title compound.

後処理

  1. additionwere added
  2. stirringthe resulting mixture was stirred at room temperature for 16 hours
  3. extractionthe mixture was extracted with diethyl ether (3×20 ml)
  4. washThe combined organic extracts were washed with saturated aqueous ammonium chloride (20 ml)
  5. dry with materialdried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified by column chromatography over silica gel eluting with a mixture of ethyl acetate and heptane (1:2)
  8. concentrationconcentrated in vacuo
  9. customThe residue was crystallised from a mixture of methyl tert-butyl ether and heptane

出典と根拠

ORDレコード
ord-9efe03e4df4c450e9631c7f33b973282
出典データセット
uspto-grants-2001_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06177443B1

反応ノート

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