2,3-dimethyl-1H-indol-5-amine → 2-Morpholin-4-yl-6-(2-morpholin-4-yl-ethoxy)-pyrimidine-4-carboxylic acid (2,3-dimethyl-1H-indol-5-yl)-amide

HRID 641171

反応式

HRID 641171 の反応式
C[O:2][C:3]([C:5]1[CH:10]=[C:9]([O:11][CH2:12][CH2:13][N:14]2[CH2:19][CH2:18][O:17][CH2:16][CH2:15]2)[N:8]=[C:7]([N:20]2[CH2:25][CH2:24][O:23][CH2:22][CH2:21]2)[N:6]=1)=O.[NH2:26][C:27]1[CH:28]=[C:29]2[C:33](=[CH:34][CH:35]=1)[NH:32][C:31]([CH3:36])=[C:30]2[CH3:37].C[Al](C)C>C1(C)C=CC=CC=1>[CH3:36][C:31]1[NH:32][C:33]2[C:29]([C:30]=1[CH3:37])=[CH:28][C:27]([NH:26][C:3]([C:5]1[CH:10]=[C:9]([O:11][CH2:12][CH2:13][N:14]3[CH2:15][CH2:16][O:17][CH2:18][CH2:19]3)[N:8]=[C:7]([N:20]3[CH2:25][CH2:24][O:23][CH2:22][CH2:21]3)[N:6]=1)=[O:2])=[CH:35][CH:34]=2

参加物

5

反応物 3

HCID 2586882,3-dimethyl-1H-indol-5-amineHCID 16682925TrimethylaluminumHCID 592586512-Morpholin-4-yl-6-(2-morpholin-4-yl-ethoxy)-pyrimidine-4-carboxylic acid methyl ester

生成物 1

HCID 115766052-Morpholin-4-yl-6-(2-morpholin-4-yl-ethoxy)-pyrimidine-4-carboxylic acid (2,3-dimethyl-1H-indol-5-yl)-amide

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒2 回

実験手順

To a stirred mixture of compound (I) (1.02 g, 2.9 mmol) and 5-amino-2,3-dimethyl indole (488 mg, 3.04 mmol) in toluene (6.9 mL) that was heated briefly until components partly dissolved and cooled to ambient temperature, was added 2 M solution of trimethylaluminum in toluene (2.32 mL, 1.6 eq) drop-wise under nitrogen purge. Reaction mixture was stirred until bubbling (gas evolution) completed, and then heated at 115° C. (oil bath) for 15 minutes. To a cooled reaction mixture chloroform and 1 N NaOH were added, chloroform layer was separated, washed twice with water, brine and dried over anhydrous sodium sulfate. Flash column chromatography on silica gel (eluent dichloromethane-acetone-methanol (3:1:01)) and recrystallization from chloroform-ethyl acetate mixture afforded target amide, 2-Morpholin-4-yl-6-(2-morpholin-4-yl-ethoxy)-pyrimidine-4-carboxylic acid (2,3-dimethyl-1H-indol-5-yl)-amide, as a pale yellow solid (1.1 g, 79%).

後処理

  1. temperaturewas heated briefly until components
  2. dissolutionpartly dissolved
  3. custompurge
  4. customReaction mixture
  5. customuntil bubbling (gas evolution)
  6. temperatureheated at 115° C. (oil bath) for 15 minutes
  7. customTo a cooled reaction mixture chloroform and 1 N NaOH
  8. additionwere added
  9. customchloroform layer was separated
  10. washwashed twice with water, brine
  11. dry with materialdried over anhydrous sodium sulfate
  12. customFlash column chromatography on silica gel (eluent dichloromethane-acetone-methanol (3:1:01)) and recrystallization from chloroform-ethyl acetate mixture

出典と根拠

ORDレコード
ord-ab29fdc273e34ee08904fc56ebbde88b
出典データセット
uspto-grants-2010_04
特許番号
US07696202B2

関連ノート

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