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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → HCID 44242067、化合物

HRID 1446055
ノート
印刷プレビュー

反応式

HRID 1446055 の反応式
[F:1][C:2]1[CH:3]=[C:4]([N:38]2[CH2:42][C@H:41]([CH2:43][NH:44][C:45](=[O:47])[CH3:46])[O:40][C:39]2=[O:48])[CH:5]=[CH:6][C:7]=1[N:8]1[CH2:13][CH2:12][N:11]([C:14](=[O:37])[CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]([CH2:23][O:24][CH:25]3[CH2:30][O:29][C:28]4=[N:31][C:32]([N+:34]([O-:36])=[O:35])=[CH:33][N:27]4[CH2:26]3)=[CH:19][CH:18]=2)[CH2:10][CH2:9]1.C(OC(=O)COC1C=CC(CO[C@@H]2COC3=NC([N+]([O-])=O)=CN3C2)=CC=1)(C)(C)C.FC1C=C(N2CC(CNC(=O)C)OC2=O)C=CC=1N1CCNCC1.C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.CCN(C(C)C)C(C)C>C(O)(C(F)(F)F)=O.C(Cl)Cl.C(Cl)Cl>[F:1][C:2]1[CH:3]=[C:4]([N:38]2[CH2:42][C@H:41]([CH2:43][NH:44][C:45](=[O:47])[CH3:46])[O:40][C:39]2=[O:48])[CH:5]=[CH:6][C:7]=1[N:8]1[CH2:9][CH2:10][N:11]([C:14](=[O:37])[CH2:15][O:16][C:17]2[CH:18]=[CH:19][C:20]([CH2:23][O:24][C@@H:25]3[CH2:30][O:29][C:28]4=[N:31][C:32]([N+:34]([O-:36])=[O:35])=[CH:33][N:27]4[CH2:26]3)=[CH:21][CH:22]=2)[CH2:12][CH2:13]1
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 6

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 18939356N-[[3-(3-Fluoro-4-(piperazin-1-YL)phenyl)-2-oxooxazolidin-5-YL]methyl]acetamideHCID 68545750HCID 68545750、化合物HCID 68549864HCID 68549864、化合物

生成物 1

HCID 44242067HCID 44242067、化合物収率 4%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒HCID 21863450Trifluoroacetic acid methylene chloride溶媒

実験手順

(S)—N-{3-[3-Fluoro-4-(4-{2-[4-(2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6-yloxymethyl)-phenoxy]-acetyl}-piperazin-1-yl)-phenyl]-2-oxo-oxazolidin-5-ylmethyl}-acetamide. A solution of [4-(2-nitro-6,7-dihydro-5H-imidazo[2,1-b][1,3]oxazin-6(S)-yloxylmethyl)-phenoxy]-acetic acid tert-butyl ester (100 mg, 0.25 mmol) in TFA/CH2Cl2 (2 mL) was stirred at room temperature for 2 h. The resultant mixture was concentrated in vacuo, and diluted with DCM, to the solution was added N-[3-(3-fluoro-4-piperazin-1-yl-phenyl)-2-oxo-oxazolidin-5-ylmethyl]-acetamide (50 mg, 0.15 mmol) (prepared by following the procedure disclosed by U.S. Pat. No. 5,547,950 or Brickner 1996), HOBt (21.6 mg, 0.16 mmol), EDCI (30.7 mg, 0.16 mmol) and DIPEA (0.20 ml). The mixture was stirred at room temperature for 24 hours diluted with DCM, washed with sat. NaHCO3, 1 N HCl and sat. NaHCO3, dried over sodium sulfate, and concentrated in vacuo. The crude product was purified by preparative TLC plates (5% MeOH in dichloromethane) to give the title product as a solid (6.0 mg, 4%). ESI MS m/z 668.4 (M+H+).

後処理

  1. concentrationThe resultant mixture was concentrated in vacuo
  2. additiondiluted with DCM, to the solution
  3. customprepared
  4. washwashed with sat. NaHCO3, 1 N HCl and sat. NaHCO3
  5. dry with materialdried over sodium sulfate
  6. concentrationconcentrated in vacuo
  7. customThe crude product was purified by preparative TLC plates (5% MeOH in dichloromethane)

出典と根拠

ORDレコード
ord-ecea4fecde974d2aa381629b03466048
出典データセット
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07666864B2

反応ノート

読み込み中…

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