Hydrochloric Acid → 2-Chloro-(1,3)thiazolo(4,5-b)pyridine

HRID 70142

반응식

HRID 70142 반응식
[NH2:1][C:2]1[C:7](Br)=[CH:6][CH:5]=[CH:4][N:3]=1.O(CC)[C:10]([S-:12])=S.[K+].[ClH:16]>CN(C=O)C>[Cl:16][C:10]1[S:12][C:7]2[C:2]([N:1]=1)=[N:3][CH:4]=[CH:5][CH:6]=2

참가 물질

5

실험 절차

2-Amino-3-bromopyridine (1.0 g, 5.8 mmol) and potassium ethyl xanthate (2.22 g, 13.9 mmol) were heated to 130° C. in DMF (5 mL) overnight. After cooling to rt, the reaction mixture was diluted with 1 M aqueous HCl (30 mL) and stirred at rt for an additional 1 h. The resulting solid was collected by filtration, washed with water (2×), and air-dried. The material was suspended in CH2Cl2 (2 mL) and sulfuryl chloride (5 mL) was added. After 2 h, water (30 mL) was added to decompose the excess sulfuryl chloride. The reaction mixture was diluted with EtOAc (30 mL) and washed with water (2×) and brine. The EtOAc layer was discarded. The combined aqueous washes were brought to pH ˜12 with 1 N aqueous NaOH and were extracted with EtOAc (3×). The combined EtOAc extracts were dried over Na2SO4, filtered, and concentrated under reduced pressure. This gave 0.933 g (95%) of the title compound as a yellow solid. LC-MS: RT=5.81 min., [M+H]+=171.1.

후처리

  1. filtrationThe resulting solid was collected by filtration
  2. washwashed with water (2×)
  3. customair-dried
  4. additionsulfuryl chloride (5 mL) was added
  5. waitAfter 2 h
  6. additionwater (30 mL) was added
  7. additionThe reaction mixture was diluted with EtOAc (30 mL)
  8. washwashed with water (2×) and brine
  9. extractionwere extracted with EtOAc (3×)
  10. dry with materialThe combined EtOAc extracts were dried over Na2SO4
  11. filtrationfiltered
  12. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-daa3ea91cf524e27b73f2ed451cffce0
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08822472B2

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