Water → 13-(2-Cyanoethyl)-6,7,12,13-tetrahydro-3-hydroxy-12-methyl-5,7-dioxo-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole

HRID 1418631

反応式

HRID 1418631 の反応式
[C:1]([CH2:3][CH2:4][N:5]1[C:13]2[C:14]3[N:15]([CH3:29])[C:16]4[C:21]([C:22]=3[C:23]3[CH2:27][NH:26][C:25](=[O:28])[C:24]=3[C:12]=2[C:11]2[CH:10]=[C:9]([O:30]C)[CH2:8][C:7](=O)[C:6]1=2)=[CH:20][CH:19]=[CH:18][CH:17]=4)#[N:2].B(Br)(Br)Br.O.C([O:41]C(C)C)(C)C.CC(C)=O>ClCCl.O1CCCC1>[C:1]([CH2:3][CH2:4][N:5]1[C:13]2[C:14]3[N:15]([CH3:29])[C:16]4[C:21]([C:22]=3[C:23]3[C:27](=[O:41])[NH:26][C:25](=[O:28])[C:24]=3[C:12]=2[C:11]2[CH:10]=[C:9]([OH:30])[CH:8]=[CH:7][C:6]1=2)=[CH:20][CH:19]=[CH:18][CH:17]=4)#[N:2]

参加物

7

反応物 4

HCID 962WaterHCID 25134Boron tribromide2 回HCID 22221350Acetone diisopropyl etherHCID 8675390513-(2-cyanoethyl)-6,7,12,13-tetrahydro-3-methoxy-12-methyl-5,1-dioxo-5H-indolo-[2,3-a]pyrrolo[3,4-c]carbazole

生成物 1

HCID 2121685613-(2-Cyanoethyl)-6,7,12,13-tetrahydro-3-hydroxy-12-methyl-5,7-dioxo-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒2 回HCID 8028Tetrahydrofuran溶媒

反応条件

温度
20 °C

実験手順

200 mg (0.45 mmol) 13-(2-cyanoethyl)-6,7,12,13-tetrahydro-3-methoxy-12-methyl-5,1-dioxo-5H-indolo-[2,3-a]pyrrolo[3,4-c]carbazole (Example 1) in 15 ml dichloromethane are cooled to -10° C. and 0.1 ml (0.7 mmol) of a 1M solution of boron tribromide in dichloromethane added dropwise thereto. Since, after 3 hours at -10° C., no reaction is shown (TLC), 1.4 ml of the 1M solution of boron tribromide are again added thereto, followed by stirring for 16 hours at 20° C. 100 ml of water and 100 ml tetrahydrofuran are added thereto and the organic phase is separated off, washed with 100 ml of water and dried over anhydrous sodium sulphate. After filtration and evaporation, the residue is first chromatographed with dichloro-methane/methanol (95:5 v/v) and then again with toluene/tetrahydrofuran (4:1 v/v). The fraction with the Rf 0.3 in toluene/tetrahydrofuran (2:1 v/v) is isolated, stirred with diisopropyl ether/acetone and the crystals formed are filtered off. 13-(2-Cyanoethyl)-6,7,12,13-tetrahydro-3-hydroxy-12-methyl-5,7-dioxo-5H-indolo[2,3-a]pyrrolo[3,4-c]carbazole is obtained in the form of yellow crystals which decompose from about 315° C.

後処理

  1. additionare again added
  2. customthe organic phase is separated off
  3. washwashed with 100 ml of water
  4. dry with materialdried over anhydrous sodium sulphate
  5. filtrationAfter filtration and evaporation
  6. customthe residue is first chromatographed with dichloro-methane/methanol (95:5 v/v)
  7. customThe fraction with the Rf 0.3 in toluene/tetrahydrofuran (2:1 v/v) is isolated
  8. customthe crystals formed
  9. filtrationare filtered off

出典と根拠

ORDレコード
ord-11e8040c73dc47efa63a29585f7f0297
出典データセット
uspto-grants-1999_03
特許番号
US05883114

関連ノート

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