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Ethyl orthoformate → HCID 178479638, 화합물

HRID 1701794
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HRID 1701794 반응식
[ClH:1].Cl.[NH2:3][CH2:4][C:5]([C:7]1[N:8]=[CH:9][NH:10][C:11]=1[NH2:12])=[O:6].[CH:13](OCC)(OCC)OCC>C(O)C>[ClH:1].[N:8]1[C:7]2[C:5](=[O:6])[CH2:4][NH:3][CH:13]=[N:12][C:11]=2[NH:10][CH:9]=1
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참가 물질

4

반응물 2

HCID 31214Ethyl orthoformateHCID 178478705HCID 178478705, 화합물

생성물 1

HCID 178479638HCID 178479638, 화합물

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of 285 mg. of 2-amino-1-(5-amino-1H-imidazol-4-yl)ethanone dihydrochloride (Example 1), 200 ml. of absolute ethanol and 10 ml. of triethyl orthoformate is stirred and heated at reflux for 1 hour, then cooled and evaporated at reduced pressure. The residue of 6,7-dihydroimidazo[4,5-d][1,3]diazepin-8(3H)-one monohydrochloride, which crystallizes on standing, is collected by filtration, washed with ethanol, then with ether, and dried at reduced pressure; m.p. above 250° C. dec.

후처리

  1. additionA mixture of 285 mg
  2. temperatureheated
  3. temperatureat reflux for 1 hour
  4. temperaturecooled
  5. customevaporated at reduced pressure
  6. customThe residue of 6,7-dihydroimidazo[4,5-d][1,3]diazepin-8(3H)-one monohydrochloride, which crystallizes on standing
  7. filtrationis collected by filtration
  8. washwashed with ethanol
  9. dry with materialwith ether, and dried at reduced pressure

출처 및 근거

ORD 기록
ord-2ec054efa5c8411fa5078572ef6aab43
출처 데이터셋
uspto-grants-1980_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04195176

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