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1H-Indole-3-propanoic acid → (2.3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[3-(1H-indol-3-yl)-propyl]-amine

HRID 1290261
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HRID 1290261 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH2:10][CH2:11][C:12](O)=O)=[CH:2]1.O.ON1C2C=CC=CC=2N=N1.C(N=C=NC(C)C)(C)C.Cl.[O:36]1[C:41]2[CH:42]=[CH:43][CH:44]=[CH:45][C:40]=2[O:39][CH2:38][CH:37]1[CH2:46][NH2:47]>CN(C=O)C>[O:36]1[C:41]2[CH:42]=[CH:43][CH:44]=[CH:45][C:40]=2[O:39][CH2:38][CH:37]1[CH2:46][NH:47][CH2:12][CH2:11][CH2:10][C:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[NH:1][CH:2]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 37441H-Indole-3-propanoic acidHCID 12734DiisopropylcarbodiimideHCID 27960291-Hydroxybenzotriazole hydrateHCID 28498361,4-Benzodioxan, 2-(aminomethyl)-, hydrochloride

생성물 1

HCID 18923870(2.3-Dihydro-benzo[1,4]dioxin-2-ylmethyl)-[3-(1H-indol-3-yl)-propyl]-amine수율 62%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매
2회

실험 절차

3-Indolepropionic acid (1.1 g, 6.0 mmole), 1-hydroxybenzotriazole hydrate (0.97 g, 7.2 mmole) and 1,3-diisopropylcarbodiimide (2.3 ml, 14.4 mmole) were combined in 100 ml of DMF and stirred at room temperature for 2 hours under a nitrogen atmosphere. To this was added dropwise 2,3-dihydro-1,4-benzodioxin-2-methanamine hydrochloride (1.2 g, 6.0 mmole) in 50 ml of DMF, and the mixture was further stirred for 24 hours. The solvent was removed and the residue partitioned between dichloromethane and water. The separated dichloromethane layer was dried over anhydrous sodium sulfate, filtered and concentrated in vacuum. The residue was chromatographed on a silica gel column using ethyl acetate as the eluant. Fractions containing product were concentrated and washed with a minimum amount of THF to remove a by-product and to give 1.2 g (60%) of the desired product, (2,3-dihydrobenzo[1,4]dioxin-2-ylmethyl)-4-(1H-indol-3-yl)-propanamide, as an oily solid.

후처리

  1. stirringthe mixture was further stirred for 24 hours
  2. customThe solvent was removed
  3. customthe residue partitioned between dichloromethane and water
  4. dry with materialThe separated dichloromethane layer was dried over anhydrous sodium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated in vacuum
  7. customThe residue was chromatographed on a silica gel column
  8. additionFractions containing product
  9. concentrationwere concentrated
  10. washwashed with a minimum amount of THF
  11. customto remove a by-product

출처 및 근거

ORD 기록
ord-b52a2b3c0a8e4215b363f35511ac5223
출처 데이터셋
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05750724

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