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Water → HCID 20450012, 화합물

HRID 358068
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HRID 358068 반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:11][C:10](=O)[CH2:9][CH2:8][CH:7]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[F:19])[C:6]=2[CH:20]=1.COC1C=CC([SH:29]2(=S)PP(=S)(C3C=CC(OC)=CC=3)S2)=CC=1.O>CN(C)P(=O)(N(C)C)N(C)C>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:11][C:10](=[S:29])[CH2:9][CH2:8][CH:7]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[F:19])[C:6]=2[CH:20]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 20449988HCID 20449988, 화합물HCID 178492777HCID 178492777, 화합물

생성물 1

HCID 20450012HCID 20450012, 화합물

시약·촉매·용매 1

HCID 12679Hexamethylphosphoramide용매

실험 절차

30 g of 7-chloro-5-(2-fluorophenyl)-1,3,4,5-tetrahydro-2H-1-benzazepin-2-one are dissolved in 105 ml of hexamethylphosphoric acid triamide and treated with 22 g of 2,4-bis-(4-methoxyphenyl)-1,2,3,4-dithiadiphosphetane-2,4-disulphide. The mixture is heated to 100° for 1 hour, again cooled to room temperature and poured into 1.41 l of water. The mixture is extracted four times with ethyl acetate and the organic extracts are washed with water. The ethyl acetate solution is dried, filtered and evaporated in vacuo. After crystallization of the residue from ethanol, there is obtained 7-chloro-5-(2-fluorophenyl)-1,3,4,5-tetrahydro-2H-1-benzazepine-2-thione of melting point 190°.

후처리

  1. temperatureThe mixture is heated to 100° for 1 hour
  2. extractionThe mixture is extracted four times with ethyl acetate
  3. washthe organic extracts are washed with water
  4. dry with materialThe ethyl acetate solution is dried
  5. filtrationfiltered
  6. customevaporated in vacuo
  7. customAfter crystallization of the residue from ethanol

출처 및 근거

ORD 기록
ord-db93c53b00ce438f9d390fcaf0d935c9
출처 데이터셋
uspto-grants-1984_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04464300

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