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Sodium borohydride → (+/-)-7-Chloro-1,2-dimethyl-4H-benzo[5,6]cyclohepta[1,2-d]imidazol-4-ol

HRID 324483
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HRID 324483 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[C:16](=[O:17])[C:10]3[N:11]=[C:12]([CH3:15])[N:13]([CH3:14])[C:9]=3[CH:8]=[CH:7][C:6]=2[CH:18]=1.[BH4-].[Na+]>C(O)C.ClCCl>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[CH:16]([OH:17])[C:10]3[N:11]=[C:12]([CH3:15])[N:13]([CH3:14])[C:9]=3[CH:8]=[CH:7][C:6]=2[CH:18]=1
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참가 물질

5

반응물 2

HCID 4311764Sodium borohydrideHCID 220035787-Chloro-1,2-dimethyl-4H-benzo[5,6]cyclohepta[1,2-d]imidazol-4-one

생성물 1

HCID 22003588(+/-)-7-Chloro-1,2-dimethyl-4H-benzo[5,6]cyclohepta[1,2-d]imidazol-4-ol

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6344Dichloromethane용매

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온도
50 °C
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실험 절차

A mixture of the product from step (ii) (1.43 g), and sodium borohydride (0.42 g) in ethanol (100 ml) and dichloromethane (20 ml) were heated at 50° C. for 4 h. The solvents were evaporated under reduced pressure and the residue was dissolved in dichloromethane, washed with dilute aqueous sodium hydroxide solution, dried (CaCl2), and evaporated to give the subtitled product as a brown solid.

후처리

  1. customThe solvents were evaporated under reduced pressure
  2. dissolutionthe residue was dissolved in dichloromethane
  3. washwashed with dilute aqueous sodium hydroxide solution
  4. dry with materialdried (CaCl2)
  5. customevaporated

출처 및 근거

ORD 기록
ord-680b5f8b98954f02be172cf03af1e864
출처 데이터셋
uspto-grants-2001_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06218376B1

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