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Diisopropylethylamine → (1-[4-(6-Chloro-1H-indol-2-yl)-benzyl]-3,5-dimethyl-1H-pyrazol-4-yl)-acetic acid

HRID 1500401
ノート
印刷プレビュー

反応式

HRID 1500401 の反応式
C([O:5][C:6](=[O:24])[CH2:7][C:8]1[C:9]([CH3:23])=[N:10][N:11]([CH2:14][C:15]2[CH:20]=[CH:19][C:18]([C:21]#[CH:22])=[CH:17][CH:16]=2)[C:12]=1[CH3:13])(C)(C)C.[Cl:25][C:26]1[CH:27]=[CH:28][C:29](I)=[C:30]([NH2:32])[CH:31]=1.C(N(C(C)C)CC)(C)C>O1CCCC1.CN1CCCC1=O>[Cl:25][C:26]1[CH:31]=[C:30]2[C:29]([CH:22]=[C:21]([C:18]3[CH:17]=[CH:16][C:15]([CH2:14][N:11]4[C:12]([CH3:13])=[C:8]([CH2:7][C:6]([OH:5])=[O:24])[C:9]([CH3:23])=[N:10]4)=[CH:20][CH:19]=3)[NH:32]2)=[CH:28][CH:27]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 81531DiisopropylethylamineHCID 6396975-Chloro-2-iodoanilineHCID 867165361-(4-ethynylbenzyl)-3,5-dimethyl-1H-pyrazol-4-yl-acetic acid tert.-butyl ester

生成物 1

HCID 66550737(1-[4-(6-Chloro-1H-indol-2-yl)-benzyl]-3,5-dimethyl-1H-pyrazol-4-yl)-acetic acid収率 37.9%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒
HCID 13387N-methyl-2-pyrrolidone溶媒

反応条件

温度
50 °C

実験手順

To a stirred solution of 1-(4-ethynylbenzyl)-3,5-dimethyl-1H-pyrazol-4-yl-acetic acid tert.-butyl ester (4.4 g) and 5-chloro-2-iodophenylamine (3.4 g) in tetrahydrofuran (100 ml) at room temperature is added diisopropylethylamine (5.8 ml). The reaction is degassed and put under argon. Copper(I)iodide (260 mg) and bis(triphenylphosphine)palladiumdichloride (475 mg) are added. After 18 h, the reaction mixture is absorbed onto Extrelut and purified by flash chromatography (7:3 isocratic-cyclohexane:ethyl acetate) to yield a solid (4.3 g; HPLC retention time 1.66 min (Method J)). The solid (4.2 g) is dissolved in N-methyl-2-pyrrolidone (25 ml) and the solution degassed and put under argon. Potassium tert-butoxide (4.1 g) is added and the reaction is then heated to 50° C. After 15 h, further potassium tert-butoxide (1.0 g) is added. After 15 h the reaction temperature is increased to 75° C. After 3 h, the reaction mixture is allowed to cool to room temperature and a copious amount of water is added. The reaction mixture is extracted twice with ethyl acetate and the aqueous phase is acidified to pH 3 with 1M aqueous hydrochloric acid. The resultant precipitate is filtered off and triturated with hot acetonitrile to yield (1-[4-(6-Chloro-1H-indol-2-yl)-benzyl]-3,5-dimethyl-1H-pyrazol-4-yl)-acetic acid (2.0 g; [M+H]=394; HPLC retention time 1.51 min (Method E)).

後処理

  1. customThe reaction is degassed
  2. additionCopper(I)iodide (260 mg) and bis(triphenylphosphine)palladiumdichloride (475 mg) are added
  3. customthe reaction mixture is absorbed onto Extrelut
  4. custompurified by flash chromatography (7:3 isocratic-cyclohexane:ethyl acetate)
  5. customto yield a solid (4.3 g; HPLC retention time 1.66 min (Method J))
  6. customthe solution degassed
  7. additionPotassium tert-butoxide (4.1 g) is added
  8. waitAfter 15 h
  9. additionfurther potassium tert-butoxide (1.0 g) is added
  10. temperatureAfter 15 h the reaction temperature is increased to 75° C
  11. waitAfter 3 h
  12. temperatureto cool to room temperature
  13. additiona copious amount of water is added
  14. extractionThe reaction mixture is extracted twice with ethyl acetate
  15. filtrationThe resultant precipitate is filtered off
  16. customtriturated with hot acetonitrile

出典と根拠

ORDレコード
ord-048d893319eb4c418806a936cbc089f4
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09206164B2

反応ノート

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