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N-Methyl-2,2'-diaminodiethylamine → 6-chloropyrazine-2-carboxamide

HRID 1165439
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HRID 1165439 반응식
NCCN(C)CCN.N[C:10]1[C:11]([C:18]([N:20]2C=CN=C2)=[O:19])=[N:12][C:13]([Cl:17])=[C:14](N)[N:15]=1>O1CCCC1>[Cl:17][C:13]1[N:12]=[C:11]([C:18]([NH2:20])=[O:19])[CH:10]=[N:15][CH:14]=1
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참가 물질

4

반응물 2

HCID 430288N-Methyl-2,2'-diaminodiethylamineHCID 13020010(3,5-diamino-6-chloropyrazin-2-yl)(1H-imidazol-1-yl)methanone

생성물 1

HCID 12825296-chloropyrazine-2-carboxamide

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a stirred solution of 84.0 g (0.744 mol) of N-(2-aminoethyl)-N-methyl-1,2-ethanediamine (see U.S. Pat. No. 3,201,472 for an example of how to obtain this material) in 700 ml of tetrahydrofuran was added 88.6 g (0.372 mol) of 1-(3,5-diamino-6-chloropyrazinoyl)imidazole in 10 portions over 1.5 hours. After 1 hour at ambient temperature the reaction mixture was filtered and concentrated to 300 ml. The solution was added dropwise to 1.4 liters of ether with vigorous stirring. The solid was filtered, washed with ether and dried. There was obtained 74.3 g (0.258 mol, 70%) of 3,5-diamino-N-2-[(2-aminoethyl)methylamino]ethyl]-6-chloropyrazinecarboxamide. A sample was filtered through a pad of silica gel and eluted with 5:95 (v/v) methanol:methylene chloride saturated wth ammonia gas; mp 138°-139.5° C.

후처리

  1. filtrationAfter 1 hour at ambient temperature the reaction mixture was filtered
  2. concentrationconcentrated to 300 ml
  3. additionThe solution was added dropwise to 1.4 liters of ether with vigorous stirring
  4. filtrationThe solid was filtered
  5. washwashed with ether
  6. customdried

출처 및 근거

ORD 기록
ord-4087a0faaa5647cf920659a9438cc31b
출처 데이터셋
uspto-grants-1990_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04910202

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