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Diethyl Ether → 8-bromo-5-methyl-2,3,5,6-tetrahydropyrido[2,3-b][1,5]diazocin-4(1H)-one

HRID 1880009
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HRID 1880009 반응식
[Br:1]Br.[CH3:3][N:4]1[C:11](=[O:12])[CH2:10][CH2:9][NH:8][C:7]2[N:13]=[CH:14][CH:15]=[CH:16][C:6]=2[CH2:5]1.C(OCC)C>C(O)(=O)C>[Br:1][C:15]1[CH:14]=[N:13][C:7]2[NH:8][CH2:9][CH2:10][C:11](=[O:12])[N:4]([CH3:3])[CH2:5][C:6]=2[CH:16]=1
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참가 물질

5

반응물 3

HCID 3283Diethyl EtherHCID 24408BromineHCID 593328875-Methyl-2,3,5,6-tetrahydropyrido[2,3-b][1,5]diazocin-4(1h)-one

생성물 1

HCID 593328748-bromo-5-methyl-2,3,5,6-tetrahydropyrido[2,3-b][1,5]diazocin-4(1H)-one

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

Bromine (189 μL, 3.7 mmol) was added to a solution of 5-methyl-2,3,5,6-tetrahydropyrido[2,3-b][1,5]diazocin-4(1H)-one (460 mg, 2.4 mmol) in 10 mL of acetic acid and stirred at room temperature for 17 h. Add 30 mL of diethyl ether and collect orange solid product via suction filtration. Redissolve the solid in DCM and wash with NaHCO3, dry the organic layer over MgSO4, and concentrate in vacuo to obtain orange solid product. Yield 670 mg (quant); 1H NMR (400 MHz, CDCl3) δ 8.10 (d, J=2.0 Hz, 1H), 7.50 (d, J=2.4 Hz, 1H), 5.17 (bs, 1H), 4.49 (s, 2H), 3.59 (bm, 2H), 3.04 (t, J=6.8 Hz, 2H), 2.85 (s, 3H); ESI MS m/z 270, 272 [C10H12N3OBr+H]+

후처리

  1. customcollect orange solid product
  2. filtrationvia suction filtration
  3. dissolutionRedissolve the solid in DCM
  4. washwash with NaHCO3
  5. dry with materialdry the organic layer over MgSO4
  6. concentrationconcentrate in vacuo
  7. customto obtain orange solid product

출처 및 근거

ORD 기록
ord-fcec3cbb3acc44a7a1180bb3039d2011
출처 데이터셋
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08318720B2

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