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Hydrochloric Acid → HCID 178499043, 화합물

HRID 973829
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HRID 973829 반응식
[NH2:1][C:2]1[N:6]=[C:5]([C:7]([O:9][CH3:10])=[O:8])[NH:4][N:3]=1.O=[C:12]([CH:19]([CH3:21])[CH3:20])[CH2:13][C:14](OCC)=[O:15].Cl>C(O)(=O)C>[OH:15][C:14]1[N:3]2[N:4]=[C:5]([C:7]([O:9][CH3:10])=[O:8])[N:6]=[C:2]2[N:1]=[C:12]([CH:19]([CH3:21])[CH3:20])[CH:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 77201methyl 5-amino-1H-(1,2,4)triazole-3-carboxylateHCID 81583Ethyl isobutyrylacetate

생성물 1

HCID 178499043HCID 178499043, 화합물수율 55.6%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A mixture of 3-amino-5-methoxycarbonyl-s-triazole (60 g) and ethyl 3-oxo-4-methylvalerate (65 g) in 600 ml of acetic acid was refluxed for five hours, the reaction mixture was cooled to room temperature, its pH was lowered to 1 to 2 with concentrated hydrochloric acid, and the separated crystals were recrystallized from ethanol, affording 54 g of the objective compound as colorless crystals.

후처리

  1. temperaturewas refluxed for five hours
  2. customthe separated crystals were recrystallized from ethanol

출처 및 근거

ORD 기록
ord-16fda21aaf6b4bf7adb5a27535924f20
출처 데이터셋
uspto-grants-1991_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05064953

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