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Hydrochloric Acid → 2-Ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetic acid

HRID 543833
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HRID 543833 반응식
[CH2:1]([O:3][N:4]=[C:5]([C:9]1[N:13]=[C:12]([NH:14]C=O)[S:11][N:10]=1)[C:6]([OH:8])=[O:7])[CH3:2].[OH-].[Na+].Cl>C(OCC)(=O)C>[CH2:1]([O:3][N:4]=[C:5]([C:9]1[N:13]=[C:12]([NH2:14])[S:11][N:10]=1)[C:6]([OH:8])=[O:7])[CH3:2]
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참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 537593012-Ethoxyimino-2-(5-formamido-1,2,4-thiadiazol-3-yl)acetic acid

생성물 1

HCID 543509922-Ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetic acid수율 75%

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 2-ethoxyimino-2-(5-formamido-1,2,4-thiadiazol-3-yl)acetic acid (syn isomer) (4.4 g) and 1 N aqueous solution of sodium hydroxide (54 ml) was stirred for 2 hours at 50° to 55° C. The mixture was cooled in an ice bath, acidified with hydrochloric acid (5.4 ml) and extracred with ethyl acetate. The extract was dried over magnesium sulfate and evaporated to dryness. The residue was triturated with diethyl ether to give 2-ethoxyimino-2-(5-amino-1,2,4-thiadiazol-3-yl)acetic acid (syn isomer) (2.92 g), mp. 168° to 170° C. (dec.).

후처리

  1. temperatureThe mixture was cooled in an ice bath
  2. dry with materialThe extract was dried over magnesium sulfate
  3. customevaporated to dryness
  4. customThe residue was triturated with diethyl ether

출처 및 근거

ORD 기록
ord-6b9a6bec9429434fb92086ca724621eb
출처 데이터셋
uspto-grants-1984_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04447429

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