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Sodium Acetate → HCID 58504354, 화합물

HRID 1941895
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HRID 1941895 반응식
[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:5]=[CH:4][C:3]=1[C:13]([O:15]/[N:16]=[C:17](/[C:19]1[CH:33]=[CH:32][C:22]([CH2:23][N:24]2[CH2:27][CH:26]([C:28]([O:30][CH3:31])=[O:29])[CH2:25]2)=[CH:21][CH:20]=1)\[NH2:18])=O.C([O-])(=O)C.[Na+]>CCO.O>[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=2)[N:5]=[CH:4][C:3]=1[C:13]1[O:15][N:16]=[C:17]([C:19]2[CH:33]=[CH:32][C:22]([CH2:23][N:24]3[CH2:27][CH:26]([C:28]([O:30][CH3:31])=[O:29])[CH2:25]3)=[CH:21][CH:20]=2)[N:18]=1
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참가 물질

5

반응물 2

HCID 517045Sodium AcetateHCID 58504345HCID 58504345, 화합물

생성물 1

HCID 58504354HCID 58504354, 화합물수율 71.8%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

반응 조건

온도
90 °C

실험 절차

To a suspension of (Z)-methyl 1-(4-(N′-(5-amino-1-phenyl-1H-pyrazole-4-carbonyloxy)carbamimidoyl)benzyl)azetidine-3-carboxylate (102 mg, 0.227 mmol) in EtOH (3 mL) was added sodium acetate (37.3 mg, 0.455 mmol) as a solution in water (1 mL). The mixture was heated to 90° C. for 3 hr. The reaction mixture was transferred to a microwave vial and was then heated to 120° C. for 30 minutes. The reaction mixture was partitioned between EtOAc (30 mL) and water (30 mL). The aqueous layer was extracted with EtOAc (15 mL) and the combined organic layers were dried (MgSO4) and concentrated to afford an oil that was chromatographed on a 12 gm Isco silica gel cartridge, eluting with a 0-100% EtOAc/hexane gradient. The pure fractions were concentrated to afford methyl 1-(4-(5-(5-amino-1-phenyl-1H-pyrazol-4-yl)-1,2,4-oxadiazol-3-yl)benzyl)azetidine-3-carboxylate (70 mg, 0.163 mmol) as a colorless oil. HPLC retention time=1.35 (ethyl ester-1.42) minutes (PHENOMENEX® Luna 4.6×30 mm S-5 ODS column) eluting with 10-90% aqueous methanol+0.1% TFA over a 2 minute gradient. MS:(M+H)=431.23 (ethyl ester-445.25). (The product is a mixture of methyl ester and ethyl ester due to partial transesterification during the reaction. The mixture was carried on through the sequence.)

후처리

  1. temperaturewas then heated to 120° C. for 30 minutes
  2. customThe reaction mixture was partitioned between EtOAc (30 mL) and water (30 mL)
  3. extractionThe aqueous layer was extracted with EtOAc (15 mL)
  4. dry with materialthe combined organic layers were dried (MgSO4)
  5. concentrationconcentrated
  6. customto afford an oil that
  7. customwas chromatographed on a 12 gm Isco silica gel cartridge
  8. washeluting with a 0-100% EtOAc/hexane gradient
  9. concentrationThe pure fractions were concentrated

출처 및 근거

ORD 기록
ord-4199751dc38e42fabbaccd95acd7f3fd
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08389509B2

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