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Triphenylphosphine → HCID 178454107, 화합물

HRID 707291
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HRID 707291 반응식
[C:1]([O:5][C:6](=[O:13])[NH:7][C@H:8]1[CH2:11][C@H:10](O)[CH2:9]1)([CH3:4])([CH3:3])[CH3:2].[Br:14][C:15]1[N:20]=[C:19]2[N:21]([CH:25]3[CH2:27][CH2:26]3)[C:22](=[O:24])[NH:23][C:18]2=[N:17][CH:16]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.CC(OC(/N=N/C(OC(C)C)=O)=O)C>C1COCC1>[C:1]([O:5][C:6](=[O:13])[NH:7][C@H:8]1[CH2:11][C@H:10]([N:23]2[C:18]3=[N:17][CH:16]=[C:15]([Br:14])[N:20]=[C:19]3[N:21]([CH:25]3[CH2:26][CH2:27]3)[C:22]2=[O:24])[CH2:9]1)([CH3:4])([CH3:3])[CH3:2]
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참가 물질

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반응물 4

HCID 11776TriphenylphosphineHCID 5363146Diisopropyl azodicarboxylateHCID 86694158HCID 86694158, 화합물HCID 178454126HCID 178454126, 화합물

생성물 1

HCID 178454107HCID 178454107, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a cooled (0° C.) solution of tert-butyl(trans-3-hydroxycyclobutyl)carbamate (0.250 g, 1.335 mmol), 6-bromo-1-cyclopropyl-1H-imidazo[4,5-b]pyrazin-2(3H)-one (0.334 g, 1.309 mmol) and triphenylphosphine (0.520 g, 1.983 mmol) in THF (10 ml) was added DIAD (0.400 ml, 2.032 mmol) dropwise via syringe. After 10 min the reaction was allowed to warm to room temperature and stirred overnight. The reaction mixture was concentrated in vacuo and the residue was dissolved in MeOH/EtOAc, evaporated onto silica gel and purified by flash chromatography (Isco (25 gram)) eluting with EtOAc:hexanes (0:1-1:1) to give a light-yellow solid. ESI MS 445.9, 447.8 [M+Na].

후처리

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. dissolutionthe residue was dissolved in MeOH/EtOAc
  3. customevaporated onto silica gel
  4. custompurified by flash chromatography (Isco (25 gram))
  5. washeluting with EtOAc:hexanes (0:1-1:1)
  6. customto give a light-yellow solid

출처 및 근거

ORD 기록
ord-49e03840244c436e8fd6f5eedd8fc8bb
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174992B2

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