Hydrochloric Acid → HCID 178491594、化合物

HRID 501231

反応式

HRID 501231 の反応式
[CH3:1][O:2][C:3]1[CH:38]=[CH:37][C:6]([C:7]([NH:9][C:10]2[C:14]3[N:15]=[C:16]([C:18](=[O:29])[NH:19][C:20]([CH3:28])([C:22]4[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=4)[CH3:21])[S:17][C:13]=3[N:12](C(OC(C)(C)C)=O)[N:11]=2)=[O:8])=[CH:5][CH:4]=1.Cl.[Cl-].[Na+]>C(O)C.O1CCOCC1>[CH3:28][C:20]([NH:19][C:18]([C:16]1[S:17][C:13]2[NH:12][N:11]=[C:10]([NH:9][C:7](=[O:8])[C:6]3[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:38][CH:37]=3)[C:14]=2[N:15]=1)=[O:29])([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[CH3:21]

参加物

6

反応物 3

HCID 313Hydrochloric Acid2 回HCID 5234Sodium ChlorideHCID 68460727tert-butyl 3-(4-methoxybenzoylamino)-5-(1-methyl-1-phenylethylcarbamoyl)-1H-pyrazolo[4,3-d]thiazole-1-carboxylate

生成物 1

HCID 178491594HCID 178491594、化合物収率 76.3%

試薬・触媒・溶媒 2

HCID 702Ethanol溶媒HCID 312751,4-Dioxane溶媒2 回

反応条件

温度
25 °C

実験手順

0.16 g (0.31 mmol) of tert-butyl 3-(4-methoxybenzoylamino)-5-(1-methyl-1-phenylethylcarbamoyl)-1H-pyrazolo[4,3-d]thiazole-1-carboxylate dissolved in 7 ml of ethanol is placed in a 100 ml round-bottomed flask. 1.5 ml (6.0 mmol) of a 4M solution of hydrochloric acid in dioxane are then added and the reaction mixture is stirred for 15 hours at 25° C. A further 1.5 ml (6.0 mmol) of 4M solution of hydrochloric acid in dioxane are added and the mixture is stirred for 15 hours at 25° C. The reaction medium is then concentrated to dryness under reduced pressure (40° C.) and the residue is taken up in 30 ml of dichloromethane and 30 ml of water, and basified with 0.1N sodium hydroxide solution. The emulsion obtained is resorbed by saturation with sodium chloride. After separation of the phases by settling, the organic phase is dried over magnesium sulfate and concentrated to dryness under reduced pressure (40° C.). The residue is purified by flash chromatography (msilica=30 g; eluent: 95/5 dichloromethane/methanol). 0.103 g of N-(1-methyl-1-phenylethyl)-3-(4-methoxybenzoylamino)-1-H-pyrazolo[4,3-d]thiazole-5-carboxamide is thus obtained in the form of a cream-coloured foam. m.p.K=226° C. 1H NMR (400 MHz, DMSO-d6): δ ppm 1.70 (s, 6H); 3.86 (s, 3H); 7.09 (d, J=8.5 Hz, 2H); 7.20 (t, J=7.5 Hz, 1H); 7.30 (t, J=7.5 Hz, 2H); 7.41 (d, J=7.5 Hz, 2H); 8.07 (d, J=8.5 Hz, 2H); 8.53 (broad s, 1H); from 10.0 to 15.0 (very broad m, 2H).

後処理

  1. customis placed in a 100 ml round-bottomed flask
  2. stirringthe mixture is stirred for 15 hours at 25° C
  3. concentrationThe reaction medium is then concentrated to dryness under reduced pressure (40° C.)
  4. customThe emulsion obtained
  5. customAfter separation of the phases
  6. dry with materialthe organic phase is dried over magnesium sulfate
  7. concentrationconcentrated to dryness under reduced pressure (40° C.)
  8. customThe residue is purified by flash chromatography (msilica=30 g; eluent: 95/5 dichloromethane/methanol)

出典と根拠

ORDレコード
ord-f01c70ade3684d54a711d108e04e9a47
出典データセット
uspto-grants-2010_08
特許番号
US07772261B2

関連ノート

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