(2-(Dimethylamino)ethyl)triphenylphosphonium bromide → 3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl ester

HRID 24335

반응식

HRID 24335 반응식
C([Li])CCC.[Br-].[CH3:7][N:8]([CH3:30])[CH2:9][CH2:10][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.C(NCC)C.[Li].[CH2:37]([O:39][C:40]([C:42]1[NH:43][C:44]2[C:49]([C:50]=1[CH:51]=O)=[CH:48][CH:47]=[CH:46][CH:45]=2)=[O:41])[CH3:38]>C1COCC1>[CH2:37]([O:39][C:40]([C:42]1[NH:43][C:44]2[C:49]([C:50]=1[CH:51]=[CH:10][CH2:9][N:8]([CH3:30])[CH3:7])=[CH:48][CH:47]=[CH:46][CH:45]=2)=[O:41])[CH3:38]

참가 물질

6

반응물 4

HCID 2724136(2-(Dimethylamino)ethyl)triphenylphosphonium bromideHCID 5107764ethyl 3-formyl-1H-indole-2-carboxylateHCID 45051810Lithium diethylamineHCID 178418339Butyllithium

생성물 1

HCID 543568283-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl ester

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

Butyllithium (1.1 equiv.) was added to a suspension of (2-dimethylaminoethyl)triphenylphosphonium bromide in THF (0.2 M) at 0° C. After stirring for 30 minutes, lithium diethylamine (1.1 equiv.) was added dropwise followed by the cold suspension of 3-formyl-1H-indole-2-carboxylic acid ethyl ester (3.96 g, 18.2 mmol) in THF. The resulting orange suspension was stirred for 18 hours. The reaction was then quenched with saturated ammonium chloride and extracted with 10% MeOH in DCM. The organic layer was washed with saturated sodium bicarbonate, dried and concentrated to give 3-(3-dimethylaminopropenyl)-1H-indole-2-carboxylic acid ethyl ester as a brownish-red waxy solid.

후처리

  1. stirringThe resulting orange suspension was stirred for 18 hours
  2. customThe reaction was then quenched with saturated ammonium chloride
  3. extractionextracted with 10% MeOH in DCM
  4. washThe organic layer was washed with saturated sodium bicarbonate
  5. customdried
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-bef9feba2e844741aa8e3640f2b05a5a
출처 데이터셋
uspto-grants-2005_02
특허 번호
US06855730B2

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