2-Naphthoyl chloride → Naphthalene-2-carboxylic acid {4-[4-(6-fluoro-benzo[b]thiophen-3-yl)-[1,4]diazepan-1-yl]-butyl}-amide

HRID 1986910ノート

反応式

HRID 1986910 の反応式
[CH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[C:11](Cl)=[O:12].[F:14][C:15]1[CH:16]=[CH:17][C:18]2[C:22]([N:23]3[CH2:29][CH2:28][CH2:27][N:26]([CH2:30][CH2:31][CH2:32][CH2:33][NH2:34])[CH2:25][CH2:24]3)=[CH:21][S:20][C:19]=2[CH:35]=1>N1C=CC=CC=1.C(Cl)Cl>[F:14][C:15]1[CH:16]=[CH:17][C:18]2[C:22]([N:23]3[CH2:29][CH2:28][CH2:27][N:26]([CH2:30][CH2:31][CH2:32][CH2:33][NH:34][C:11]([C:2]4[CH:3]=[CH:4][C:5]5[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=5)[CH:1]=4)=[O:12])[CH2:25][CH2:24]3)=[CH:21][S:20][C:19]=2[CH:35]=1

参加物

4

実験手順

Add slowly a solution of 2-naphthoyl chloride (600 mg, 3.15 mmol) to a solution of 4-[4-(6-fluoro-benzo[b]thiophen-3-yl)-[1,4]diazapan-1-yl]butylamine (Example 6) (920 mg, 2.86 mmol), in pyridine-methylene chloride (10 mL,1:1), and stir the solution at room temperature overnight. Evaporate the solvent under vacuum, dissolve the residue in EtOAc and wash the organic layer with water and saturated sodium chloride solution. Combine the organic phases, dry over MgSO4 and evaporate the solvent under vacuum. Purify the crude product by column chromatography (EtOAc/MeOH 7:3) to obtain 1.25 g of a solid LC/MS (LiChrospher 5μ, RP-18, 250 mm CH3CN/Water-gradient 20%→100% (25 min), Flow: 1.5 mL/min) tR=21.11 min, m/z=475.3.

後処理

  1. customEvaporate the solvent under vacuum
  2. dissolutiondissolve the residue in EtOAc
  3. washwash the organic layer with water and saturated sodium chloride solution
  4. dry with materialCombine the organic phases, dry over MgSO4
  5. customevaporate the solvent under vacuum
  6. customPurify the crude product by column chromatography (EtOAc/MeOH 7:3)

出典と根拠

ORDレコード
ord-065330d01b164a3d91b4402819b85933
出典データセット
uspto-grants-2009_06
特許番号
US07550469B2

反応ノート

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