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Dimethylbarbituric acid → HCID 67401263、化合物

HRID 906641
ノート
印刷プレビュー

反応式

HRID 906641 の反応式
[CH2:1]([N:4](CC=C)[CH2:5][C:6]1[S:7][C:8]([S:11]([N:14]2[CH2:19][CH2:18][CH:17]([O:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH3:26])[CH2:16][CH2:15]2)(=[O:13])=[O:12])=[CH:9][CH:10]=1)[CH:2]=[CH2:3].CN1C(=O)CC(=O)N(C)C1=[O:33].CCN(C(C)C)C(C)C.[C:50](Cl)(=O)[C:51]1C=CC=[C:53]([O:57][CH3:58])[CH:52]=1>C(Cl)Cl.C1C=CC([P]([Pd]([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)([P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[P](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.CCOC(C)=O>[CH2:21]([O:20][CH:17]1[CH2:18][CH2:19][N:14]([S:11]([C:8]2[S:7][C:6]([CH2:5][NH:4][C:1](=[O:33])[C:2]3[CH:3]=[CH:50][CH:51]=[CH:52][C:53]=3[O:57][CH3:58])=[CH:10][CH:9]=2)(=[O:12])=[O:13])[CH2:15][CH2:16]1)[CH2:22][CH2:23][CH2:24][CH2:25][CH3:26]
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 4

HCID 69860Dimethylbarbituric acidHCID 74374m-Anisoyl chlorideHCID 81531DiisopropylethylamineHCID 67401054HCID 67401054、化合物

生成物 1

HCID 67401263HCID 67401263、化合物収率 37%

試薬・触媒・溶媒 3

HCID 178418397
HCID 178418397、化合物
触媒
HCID 6344Dichloromethane溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

A solution of 326a (134 mg, 0.3 mmol), 1,3 Dimethylbarbituric acid (94 mg, 0.6 mmol) and Tetrakis(triphenylphosphine)palladium (12 mg, 0.01 mmol) were stirred under Argon in 3 mL CH2Cl2. The reaction was followed by HPLC until all starting material disappeared. The crude was evaporated to dryness and taken up in dry THF. To this solution was added DIEA (230 ul, 1.5 mmol) and 3-anisoylchloride 0.3 mmol). The reaction was stirred for 3 h, EtOAc was added and the organic layer was extracted with NaHCO3 sat, HCl (0.1N) and brine. The dry solution was evaporated and purified by flash chromatography on silica gel using cyclohexane/EtOAc 7:3 as eluent. 326 was obtained as an oil (54 mg, 37%): H1 NMR (CDCl3) δ 7.43-7.25 (m, 4H), 7.15-7.05 (m, 2H), 6.60 (m, 1H), 4.83 (d, J=6.0 Hz, 2H), 3.86 (s, 3H), 3.35 (d, J=6.6, 2H), 335-3.23 (m, 3H), 2.95 (m, 2H), 1.94 (m, 2H), 1.86 (m, 2H), 1.70-1.50 (m, 5H), 1.30-1.20 (m, 8H), 0.87 (t, J=6.8, 3H), M/Z APCI: 495.2 (M+1).

後処理

  1. customThe crude was evaporated to dryness
  2. extractionthe organic layer was extracted with NaHCO3
  3. customThe dry solution was evaporated
  4. custompurified by flash chromatography on silica gel

出典と根拠

ORDレコード
ord-619504d190014e88b882fa3e5b8944a8
出典データセット
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08012995B1

反応ノート

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