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Trifluoroacetic acid → HCID 58864314、化合物

HRID 1353527
ノート
印刷プレビュー

反応式

HRID 1353527 の反応式
[CH3:1][O:2][C:3](=[O:27])[C:4]([NH:16]C(OCC1C=CC=CC=1)=O)=[CH:5][C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([Cl:15])[CH:14]=1)[NH:11][N:10]=[CH:9]2.FC(F)(F)C(O)=O>CO>[CH3:1][O:2][C:3](=[O:27])[CH:4]([NH2:16])[CH2:5][C:6]1[CH:7]=[C:8]2[C:12](=[C:13]([Cl:15])[CH:14]=1)[NH:11][N:10]=[CH:9]2
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 6422Trifluoroacetic acidHCID 68707452Methyl 3-(7-chloro-1H-indazol-5-yl)-2-[[(phenylmethoxy)carbonyl]amino]-2-propenoate

生成物 1

HCID 58864314HCID 58864314、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A solution of 2-benzyloxycarbonylamino-3-(7-chloro-1H-indazol-5-yl)-acrylic acid methyl ester (300 mg, 0.78 mmol) in methanol (10 mL) was treated with trifluoroacetic acid (0.2 mL), flushed with nitrogen, and treated with 10% palladium on charcoal (30 mg). The flask was flushed with hydrogen and allowed to stir under an atmosphere of hydrogen. After 4 days, all starting material had been consumed. The reaction was flushed with nitrogen, filtered through celite, and concentrated. Column chromatography gave 78 mg (40%). 1H-NMR (CDCl3, 500 MHz) δ 1.31 (bs, 3H), 2.95 (dd, J=13.7, 7.9, 1H), 3.18 (dd, J=13.7, 5.2, 1H), 3.48 (s, 3H), 3.78 (dd, J=7.9, 5.2, 1H), 7.23 (s, 1H), 7.46 (s, 1H), 8.00 (s, 1H). Mass spec.: 254.06 (MH)+.

後処理

  1. customflushed with nitrogen
  2. additiontreated with 10% palladium on charcoal (30 mg)
  3. customThe flask was flushed with hydrogen
  4. customall starting material had been consumed
  5. customThe reaction was flushed with nitrogen
  6. filtrationfiltered through celite
  7. concentrationconcentrated
  8. customColumn chromatography gave 78 mg (40%)

出典と根拠

ORDレコード
ord-888adec2e1764c84bc22be279c119766
出典データセット
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07220862B2

反応ノート

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