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Methanol → 9-Chloro-5,6-dihydrobenzo[f][1,2,4]triazolo[1,5-d][1,4]oxazepine-2-carboxylic acid

HRID 1498301
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HRID 1498301 반응식
C[O:2][C:3]([C:5]1[N:14]=[C:13]2[N:7]([CH2:8][CH2:9][O:10][C:11]3[CH:18]=[C:17]([Cl:19])[CH:16]=[CH:15][C:12]=32)[N:6]=1)=[O:4].CO.O.[Li+].[OH-]>C1COCC1>[Cl:19][C:17]1[CH:16]=[CH:15][C:12]2[C:13]3[N:7]([N:6]=[C:5]([C:3]([OH:4])=[O:2])[N:14]=3)[CH2:8][CH2:9][O:10][C:11]=2[CH:18]=1
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참가 물질

6

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HCID 887MethanolHCID 962WaterHCID 3939Lithium HydroxideHCID 58204850Methyl-9-chloro-5,6-dihydrobenzo[f][1,2,4]triazolo[1,5-d][1,4]oxazepine-2-carboxylate

생성물 1

HCID 582045869-Chloro-5,6-dihydrobenzo[f][1,2,4]triazolo[1,5-d][1,4]oxazepine-2-carboxylic acid수율 89%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

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온도
25 °C

실험 절차

Methyl-9-chloro-5,6-dihydrobenzo[f][1,2,4]triazolo[1,5-d][1,4]oxazepine-2-carboxylate (0.144 g, 0.515 mmol) was dissolved in 3:2:1 THF:MeOH:H2O (5.0 mL), and treated with 4 N aqueous LiOH (0.644 mL). The mixture was stirred for 30 min at 25° C. The reaction was quenched with 1 N aq. HCl (10 mL) and the solution was extracted with EtOAc (3×20 mL). The combined organic extracts were dried with Na2SO4 and concentrated in vacuo to give 9-Chloro-5,6-dihydrobenzo[f][1,2,4]triazolo[1,5-d][1,4]oxazepine-2-carboxylic acid (89% yield)

후처리

  1. customThe reaction was quenched with 1 N aq. HCl (10 mL)
  2. extractionthe solution was extracted with EtOAc (3×20 mL)
  3. dry with materialThe combined organic extracts were dried with Na2SO4
  4. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-5badfc5ce1ff4c81bdbbf0e75af947ed
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09198918B2

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