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Iodine → HCID 76849761, 화합물

HRID 448984
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HRID 448984 반응식
[Cl:1][C:2]1[C:3]2[N:4]([CH:8]=[N:9][CH:10]=2)[CH:5]=[CH:6][N:7]=1.[Li]CCCC.CCCCCC.[I:22]I>C1COCC1>[Cl:1][C:2]1[C:3]2[N:4]([C:8]([I:22])=[N:9][CH:10]=2)[CH:5]=[CH:6][N:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 807IodineHCID 8058HexaneHCID 122404758-Chloroimidazo[1,5-a]pyrazineHCID 178418339Butyllithium

생성물 1

HCID 76849761HCID 76849761, 화합물

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
30 °C

실험 절차

To a stirred solution of 8-chloro-imidazo[1,5-a]pyrazine (200.00 mg, 1.30 mmol) in THF (10.0 mL) was slowly added n-BuLi in hexane (2.5 M, 0.62 mL, 1.55 mmol) at −78° C. under nitrogen. The resulting mixture was stirred at the same temperature for 15 min. Then to this mixture a solution of iodine (429.7 mg, 1.693 mol) in 3 mL of THF was slowly added. The mixture was allowed to warm up to 30° C. in 1 hour. Reaction was quenched by 2 mL saturated aq. solution of NH4Cl. The reaction mixture was extracted with DCM. The solvent was removed under reduced pressure and the residue was used in next step without further purification. 1H NMR (400 MHz, CDCl3) δ 7.48 (d, J=5.05 Hz, 1H), 7.71 (dd, J=5.05, 1.01 Hz, 1H), 7.94 (d, J=1.01 Hz, 1H). MS (ES+): m/z 279.86/281.90 [MH+]; HPLC: tR=2.70 min (OpenLynx, polar—5 min).

후처리

  1. customat −78° C.
  2. customReaction
  3. customwas quenched by 2 mL saturated aq. solution of NH4Cl
  4. extractionThe reaction mixture was extracted with DCM
  5. customThe solvent was removed under reduced pressure
  6. customthe residue was used in next step without further purification
  7. customHPLC: tR=2.70 min (OpenLynx, polar—5 min)

출처 및 근거

ORD 기록
ord-b439345bbed34997900af48066a6e0e1
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08481733B2

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