Ammonia → 2-Amino-4-methylpyridine-3-carbonitrile

HRID 726598노트

반응식

HRID 726598 반응식
[C:1]([C:3]([C:11]#[N:12])=[CH:4][C:5]([CH3:10])=COCC)#[N:2].[C:13](C(C#N)=CC(C)C(OCC)OCC)#N.[NH3:28]>>[NH2:28][C:11]1[C:3]([C:1]#[N:2])=[C:4]([CH3:13])[CH:5]=[CH:10][N:12]=1

참가 물질

4

반응물 3

HCID 222AmmoniaHCID 197072091,1-Dicyano-4,4-diethoxy-3-methyl-1-buteneHCID 542610241,1-Dicyano-4-ethoxy-3-methyl-1,3-butadiene

생성물 1

HCID 103968872-Amino-4-methylpyridine-3-carbonitrile

실험 절차

A solution of about 6.1 grams (0.038 mole) of a mixture of 1,1-dicyano-4-ethoxy-3-methyl-1,3-butadiene and 1,1-dicyano-4,4-diethoxy-3-methyl-1-butene in 200 mL of saturated methanolic ammonia is stirred at ambient temperature for about 15 hours. After this time the solvent is removed under reduced pressure, and the residue is partitioned between 160 mL of aqueous 1N hydrochloric acid and 160 mL of ethyl acetate. The aqueous layer is separated and poured into 160 mL of an aqueous solution saturated with sodium bicarbonate. The resultant solid is collected by filtration and dried, yielding about 2.6 grams of 2-amino-3-cyano-4-methylpyridine. Steps A and B are repeated.

후처리

  1. customAfter this time the solvent is removed under reduced pressure
  2. customthe residue is partitioned between 160 mL of aqueous 1N hydrochloric acid and 160 mL of ethyl acetate
  3. customThe aqueous layer is separated
  4. additionpoured into 160 mL of an aqueous solution saturated with sodium bicarbonate
  5. filtrationThe resultant solid is collected by filtration
  6. customdried

출처 및 근거

ORD 기록
ord-b6c2acc3fc284b55814dafbd701ae3db
출처 데이터셋
uspto-grants-1998_01
특허 번호
US05710157

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