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Tryptamine → 2-[4-dimethylamino-4-(4-fluorophenyl)cyclohexylidene]-N-[2-(1H-indol-3-yl)ethyl]acetamide

HRID 908947
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HRID 908947 반응식
ON1C2C=CC=CC=2N=N1.[NH2:11][CH2:12][CH2:13][C:14]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=2)[NH:16][CH:15]=1.CN1CCOCC1.Cl.[CH3:31][N:32]([CH3:50])[C:33]1([C:43]2[CH:48]=[CH:47][C:46]([F:49])=[CH:45][CH:44]=2)[CH2:38][CH2:37][C:36](=[CH:39][C:40](O)=[O:41])[CH2:35][CH2:34]1.C1(N=C=NC2CCCCC2)CCCCC1.[OH-].[Na+]>O.CN(C)C=O>[CH3:50][N:32]([CH3:31])[C:33]1([C:43]2[CH:44]=[CH:45][C:46]([F:49])=[CH:47][CH:48]=2)[CH2:38][CH2:37][C:36](=[CH:39][C:40]([NH:11][CH2:12][CH2:13][C:14]2[C:22]3[C:17](=[CH:18][CH:19]=[CH:20][CH:21]=3)[NH:16][CH:15]=2)=[O:41])[CH2:35][CH2:34]1
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참가 물질

9

반응물 6

HCID 1150TryptamineHCID 79724-MethylmorpholineHCID 10868DicyclohexylcarbodiimideHCID 14798Sodium HydroxideHCID 757711-HydroxybenzotriazoleHCID 67386287HCID 67386287, 화합물

생성물 1

HCID 11705178
2-[4-dimethylamino-4-(4-fluorophenyl)cyclohexylidene]-N-[2-(1H-indol-3-yl)ethyl]acetamide
수율 95%

시약·촉매·용매 2

HCID 962Water용매HCID 6228Dimethylformamide용매

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온도
0 °C

실험 절차

1-Hydroxybenzotriazole (864 mg, 6.4 mmol), tryptamine (512 mg, 3.2 mmol) and N-methylmorpholine (0.703 ml, 6.4 mmol) were added to a solution of (4-dimethylamino-4-(4-fluorophenyl)cyclohexylidene)acetic acid hydrochloride (840 mg, 3.2 mmol) in abs. dimethylformamide (25 ml) under argon. The solution was cooled to 0° C., dicyclohexylcarbodiimide (1.32 g, 6.4 mmol) was added and the mixture was stirred at RT for 4 d. Working up of the mixture was carried out by separating off the urea which had precipitated out and introducing the filtrate into a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml). Still further urea thereby precipitated out and was separated off. The filtrate was diluted with water (400 ml), 5 M sodium hydroxide solution (5 ml, 25 mmol) was added and the mixture was stored at 5° C. for 4 d. The product thereby precipitated out as a beige-coloured oily solid in a yield of 95% (1.27 mg).

후처리

  1. customby separating off the urea which
  2. customhad precipitated out
  3. additionintroducing the filtrate
  4. additioninto a mixture of saturated NaCl solution (40 ml) and saturated NaHCO3 solution (10 ml)
  5. customStill further urea thereby precipitated out and
  6. customwas separated off
  7. additionwas added
  8. waitthe mixture was stored at 5° C. for 4 d
  9. customThe product thereby precipitated out as a beige-coloured oily solid in a yield of 95% (1.27 mg)

출처 및 근거

ORD 기록
ord-dbf86c35b6574955bf25d73aa75aa925
출처 데이터셋
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08017630B2

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