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Diethyl Ether → HCID 14208239, 화합물

HRID 620574
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HRID 620574 반응식
Cl[CH:2]1[N:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[F:15])[C:6]2[CH:16]=[CH:17][CH:18]=[CH:19][C:5]=2[NH:4][C:3]1=[O:20].[NH2:21][CH2:22][C:23]1[NH:24][C:25]2[C:30]([CH:31]=1)=[CH:29][CH:28]=[CH:27][CH:26]=2.CCOCC>COCCOC>[F:15][C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[C:7]1[C:6]2[CH:16]=[CH:17][CH:18]=[CH:19][C:5]=2[NH:4][C:3](=[O:20])[CH:2]([NH:21][CH2:22][C:23]2[NH:24][C:25]3[C:30]([CH:31]=2)=[CH:29][CH:28]=[CH:27][CH:26]=3)[N:8]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 5823312-(Aminomethyl)indoleHCID 15167810HCID 15167810, 화합물

생성물 1

HCID 14208239HCID 14208239, 화합물

시약·촉매·용매 1

HCID 80711,2-Dimethoxyethane용매

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온도
25 °C

실험 절차

3-(RS)-Chloro-1,3-dihydro-5-(2-fluorophenyl)-2H-1,4-benzodiazepin-2-one (150 mg, 0.520 mmol) and 2-aminomethylindole (75.9 mg, 0.520 mmol) were combined in 1,2-dimethoxyethane (3 ml) and the mixture stirred 20 min. at 25° C. The mixture was evaporated to dryness in vacuo and the residue treated with H2O and extracted with EtOAc (3x). The combined extracts were washed with H2O (1X), dried over MgSO4, filtered and stripped to dryness in vacuo to give an orange oil which, after chromatography on silica gel (4% MeOH in CH2Cl2) provided the title compound as a white solid from ether: (m.p. 200°-202°).

후처리

  1. customThe mixture was evaporated to dryness in vacuo
  2. additionthe residue treated with H2O
  3. extractionextracted with EtOAc (3x)
  4. washThe combined extracts were washed with H2O (1X)
  5. dry with materialdried over MgSO4
  6. filtrationfiltered
  7. customto give an orange oil which

출처 및 근거

ORD 기록
ord-0bca338837ef4df09d2f63a938cd4b42
출처 데이터셋
uspto-grants-1989_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04820834

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