1,2-Dichloroethane → HCID 14208235, 화합물

HRID 620575

반응식

HRID 620575 반응식
[NH2:1][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].[CH3:21][O:22][C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[NH:28][C:27]([C:32](O)=[O:33])=[CH:26]2.C(Cl)CCl.C(N(CC)CC)C>C(Cl)Cl>[CH3:21][O:22][C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[NH:28][C:27]([C:32]([NH:1][CH:2]1[N:8]=[C:7]([C:9]3[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=3[F:15])[C:6]3[CH:16]=[CH:17][CH:18]=[CH:19][C:5]=3[NH:4][C:3]1=[O:20])=[O:33])=[CH:26]2

참가 물질

6

반응물 4

HCID 111,2-DichloroethaneHCID 8471TriethylamineHCID 204015-Methoxyindole-2-carboxylic acidHCID 156371501,3-dihydro-5-(2-fluorophenyl)-3-amino-2H-1,4-benzodiazepin-2-one

생성물 1

HCID 14208235HCID 14208235, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

3-(RS)-Amino-1,3-dihydro-5-(2-fluorophenyl)-2H-1,4-benzodiazepin-2-one (50 mg, 0.186 mmol) was suspended in 1 ml of methylene chloride. 5-Methoxyindole-2-carboxylic acid (36.9 mg, 0.207 mmol) was added to the suspension followed by the addition of 38.5 mg (0.2 mmol) of EDC. The mixture was brought to pH 8 with 60 μl of triethylamine. The solid which formed after 3 min. was filtered after 5 hours and washed with chloroform. The filtrate was applied to a 2000μ preparative TLC plate and eluted with 90:10:1 chloroform:methanol:water (CMW). The product was extracted from silica with methanol and evaporated.

후처리

  1. customThe solid which formed after 3 min.
  2. filtrationwas filtered after 5 hours
  3. washwashed with chloroform
  4. washeluted with 90:10:1 chloroform
  5. extractionThe product was extracted from silica with methanol
  6. customevaporated

출처 및 근거

ORD 기록
ord-47076ec868c1465aaf94ab3a766c862e
출처 데이터셋
uspto-grants-1989_04
특허 번호
US04820834

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