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Water → HCID 25215195、化合物

HRID 2194770
ノート
印刷プレビュー

反応式

HRID 2194770 の反応式
[C:1]([C:3]1[CH:4]=[C:5]([CH:36]=[C:37]([CH3:39])[CH:38]=1)[C:6]([C:8]1[N:13]([CH2:14][C:15]2([CH2:18][C:19]([NH:21]CC3C=CC(OC)=CC=3)=[O:20])[CH2:17][CH2:16]2)[C:12](=[O:31])[NH:11][C:10](=[O:32])[C:9]=1[CH:33]([CH3:35])[CH3:34])=[O:7])#[N:2].O>C(#N)C.C(O)(=O)C.C(OCC)(=O)C>[C:1]([C:3]1[CH:4]=[C:5]([CH:36]=[C:37]([CH3:39])[CH:38]=1)[C:6]([C:8]1[N:13]([CH2:14][C:15]2([CH2:18][C:19]([NH2:21])=[O:20])[CH2:16][CH2:17]2)[C:12](=[O:31])[NH:11][C:10](=[O:32])[C:9]=1[CH:33]([CH3:35])[CH3:34])=[O:7])#[N:2]
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 2

HCID 962WaterHCID 582034682-{1-[6-(3-cyano-5-methyl-benzoyl)-5-isopropyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl]-cyclopropyl}-N-(4-methoxy-benzyl)-acetamide

生成物 1

HCID 25215195HCID 25215195、化合物収率 80.2%

試薬・触媒・溶媒 3

HCID 176Acetic Acid溶媒HCID 6342Acetonitrile溶媒
HCID 8857
Ethyl Acetate
溶媒

実験手順

To a stirred solution of 2-{1-[6-(3-cyano-5-methyl-benzoyl)-5-isopropyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl]-cyclopropyl}-N-(4-methoxy-benzyl)-acetamide (97 mg, 0.18 mmol) in acetonitrile (4 mL) and glacial acetic acid (1 mL) at room temperature, were added ceric ammonium nitrate (201 mg, 0.36 mmol) and water (2 mL) in this order. After stirring for 20 min., the mixture was diluted with ethyl acetate, washed with water twice, dried with MgSO4, filtered, and evaporated in vacuo. The residue was purified by silica gel column chromatography (eluent, from ethyl acetate to 10% methanol in ethyl acetate) to give 59 mg (78%) of 2-{1-[6-(3-cyano-5-methyl-benzoyl)-5-isopropyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethyl]-cyclopropyl}-acetamide (85) as a white solid. m.p. 283-285° C.; 1H-NMR (500 MHz, DMSO-d6) δ 0.20-0.27 (2H, m), 0.31-0.36 (1H, m), 0.43-0.47 (1H, m), 0.99 (3H, d, J=6.8 Hz), 1.08 (3H, d, J=6.8 Hz), 2.02-2.13 (2H, m), 2.17 (1H, d, J=16.5 Hz), 2.44 (3H, s), 3.32 (1H, d, J=15.1 Hz), 3.39-3.41 (1H, m), 3.46-3.51 (1H, m), 3.79 (1H, d, J=15.1 Hz), 8.08 (1H, s), 8.19 (1H, s), 8.42 (1H, s), 11.45 (1H, s); m/z (EI) 408 (M+).

後処理

  1. washwashed with water twice
  2. dry with materialdried with MgSO4
  3. filtrationfiltered
  4. customevaporated in vacuo
  5. customThe residue was purified by silica gel column chromatography (eluent, from ethyl acetate to 10% methanol in ethyl acetate)

出典と根拠

ORDレコード
ord-990a7daf1a5c45d08482953b79a9e795
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08334295B2

反応ノート

読み込み中…

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