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Methylamine → (3S)-3-[(1-Benzothien-2-carbonitrile-7-yl)oxy]-N-methyl-3-phenyl-1-propanamine fumarate

HRID 1822985
ノート
印刷プレビュー

反応式

HRID 1822985 の反応式
I[CH2:2][CH2:3][C@H:4]([O:11][C:12]1[C:20]2[S:19][C:18]([C:21]#[N:22])=[CH:17][C:16]=2[CH:15]=[CH:14][CH:13]=1)[C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=1.[CH3:23][NH2:24].[C:25]([OH:32])(=[O:31])/[CH:26]=[CH:27]/[C:28]([OH:30])=[O:29]>O1CCCC1.CO>[C:25]([OH:32])(=[O:31])/[CH:26]=[CH:27]/[C:28]([OH:30])=[O:29].[S:19]1[C:20]2[C:12]([O:11][C@H:4]([C:5]3[CH:10]=[CH:9][CH:8]=[CH:7][CH:6]=3)[CH2:3][CH2:2][NH:24][CH3:23])=[CH:13][CH:14]=[CH:15][C:16]=2[CH:17]=[C:18]1[C:21]#[N:22]
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 6329MethylamineHCID 444972Fumaric AcidHCID 586307067-{[(1S)-3-iodo-1-phenylpropyl]oxy}-1-benzothiophene-2-carbonitrile

生成物 1

HCID 86594247(3S)-3-[(1-Benzothien-2-carbonitrile-7-yl)oxy]-N-methyl-3-phenyl-1-propanamine fumarate収率 85%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒2 回
HCID 8028
Tetrahydrofuran
溶媒

実験手順

To a solution of 7-{[(1S)-3-iodo-1-phenylpropyl]oxy}-1-benzothiophene-2-carbonitrile (222 mg, 0.5 mmol) in tetrahydrofuran (2 mL) was added 40% aqueous methylamine (0.83 mL) and the solution was stirred at room temperature for 16 hours. The solvent removed in vacuo and the residue purified by flash chromatography with a gradient of 0–15% methanol in dichloromethane. To a solution of free base (155 mg, 0.48 mmol) in methanol (1 mL) and added a warm solution of fumaric acid (40 mg, 0.48 mmol) in methanol (1 mL). The solvent removed in vacuo, and the solid residue triturated with diethyl ether (5 mL), then dried in a vacuum oven at 40° C. for 1 h to give the title compound (0.20 g, 85%); δH (300 MHz, DMSO) 8.40 (1H, s, 3-ArH), 7.61–7.52 (1H, m, ArH), 7.49–7.23 (6H, m, ArH), 7.05–6.98 (1H, m, ArH), 6.43 (2H, s, CHCO2H), 5.85–5.75 (1H, m, CHO), 3.05–2.90 (2H, m, 1-CH2), 2.52 (3H, s, NHCH3) and 2.46–2.07 (2H, m, 2-CH2).

後処理

  1. customThe solvent removed in vacuo
  2. customthe residue purified by flash chromatography with a gradient of 0–15% methanol in dichloromethane
  3. customThe solvent removed in vacuo
  4. customthe solid residue triturated with diethyl ether (5 mL)
  5. customdried in a vacuum oven at 40° C. for 1 h

出典と根拠

ORDレコード
ord-13bb0ffa870b483ba016f6a74a970b9a
出典データセット
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07037932B2

反応ノート

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