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Nitrogen → 2-(2-((4-Amino-2H-1,2,3-triazol-2-yl)methyl)oxazol-4-yl)propan-2-ol

HRID 527248
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HRID 527248 반응식
N#N.[N+:3]([C:6]1[CH:10]=[N:9][N:8]([CH2:11][C:12]2[O:13][CH:14]=[C:15]([C:17]([OH:20])([CH3:19])[CH3:18])[N:16]=2)[N:7]=1)([O-])=O.[NH4+].[Cl-]>CCO.O.[Fe]>[NH2:3][C:6]1[CH:10]=[N:9][N:8]([CH2:11][C:12]2[O:13][CH:14]=[C:15]([C:17]([OH:20])([CH3:18])[CH3:19])[N:16]=2)[N:7]=1
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참가 물질

7

반응물 3

HCID 947NitrogenHCID 25517Ammonium ChlorideHCID 67958661HCID 67958661, 화합물

생성물 1

HCID 679587652-(2-((4-Amino-2H-1,2,3-triazol-2-yl)methyl)oxazol-4-yl)propan-2-ol

시약·촉매·용매 3

HCID 23925Iron촉매HCID 702Ethanol용매
HCID 962
Water
용매

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온도
85 °C

실험 절차

In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), a mixture of 2-(2-((4-nitro-2H-1,2,3-triazol-2-yl)methyl)oxazol-4-yl)propan-2-ol (2.40 g, 10.75 mmol), iron powder (1.82 g, 32.25 mmol) and NH4Cl (2.90 g, 53.76 mmol) in a mixture of EtOH (70 mL) and water (35 mL) was stirred at 85° C. for 15 min. The reaction mixture was filtered while hot and concentrated under reduced pressure. CH2Cl2 (110 mL) was added followed by 1N NaOH (65 mL). The layers were separated and the aq. layer was extracted with CH2Cl2 (5×50 mL). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure to give the title compound as an orange oil. LC-MS-conditions 06: tR=0.35 min; [M+H]+=224.00.

후처리

  1. filtrationThe reaction mixture was filtered while hot and
  2. concentrationconcentrated under reduced pressure
  3. additionCH2Cl2 (110 mL) was added
  4. customThe layers were separated
  5. extractionthe aq. layer was extracted with CH2Cl2 (5×50 mL)
  6. dry with materialextracts were dried over MgSO4
  7. filtrationfiltered
  8. customthe solvents were removed under reduced pressure

출처 및 근거

ORD 기록
ord-249fc07b6a694ffc9423c8ed9637ac9a
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09346793B2

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