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Chloroacetyl chloride → HCID 21414251, 화합물

HRID 442326
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HRID 442326 반응식
[O-2].[Mg+2].[CH3:3][N:4]1[C:10]2[CH:11]=[CH:12][C:13]([Cl:15])=[CH:14][C:9]=2[CH:8]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[NH:7][CH2:6][C:5]1=[O:22].[Cl:23][CH2:24][C:25](Cl)=[O:26]>C(Cl)(Cl)Cl>[CH3:3][N:4]1[C:10]2[CH:11]=[CH:12][C:13]([Cl:15])=[CH:14][C:9]=2[CH:8]([C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[N:7]([C:25](=[O:26])[CH2:24][Cl:23])[CH2:6][C:5]1=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6577Chloroacetyl chlorideHCID 30819844,5-DihydrodiazepamHCID 6850729Magnesium monoxide

생성물 1

HCID 21414251HCID 21414251, 화합물수율 8.14%

시약·촉매·용매 1

HCID 6212Chloroform용매2회

실험 절차

3 g. of magnesium oxide are added to a solution of 2.87 g. (0.01 mmoles) of 1-methyl-5-phenyl-7-chloro-1,3,4,5-tetrahydro-2 H-1,4-benzodiazepine-2-one in 30 ml. of chloroform, and a solution of 1.2 ml. (0.018 moles) of chloroacetyl chloride in 4 ml. of chloroform is added to the vigorously stirred mixture. After 3 hours of stirring at room temperature the magnesium salt is filtered off, washed with 20 ml. of chloroform, and the filtrate is evaporated to dryness under reduced pressure. The residue is crystallized from acetone. 2.68 g. (8.14 %) of 1-methyl-4-chloroacetyl-5-phenyl-7-chloro-1,3,4,5-tetrahydro-2H-1,4-benzodiazepine-2-one are obtained; m.p.: 197°-200° C.; Rf2 = 0.5.

후처리

  1. filtrationis filtered off
  2. washwashed with 20 ml
  3. customof chloroform, and the filtrate is evaporated to dryness under reduced pressure
  4. customThe residue is crystallized from acetone

출처 및 근거

ORD 기록
ord-35ae73e7c4a24330bcf93181976dca51
출처 데이터셋
uspto-grants-1977_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04045433

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