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Hydrogen Bromide → 3-bromothieno[3,2-c]pyridin-6(5H)-one

HRID 389545
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HRID 389545 반응식
[Br:1][C:2]1[C:3]([CH2:7][NH:8][C:9](=[O:17])[CH:10](OCC)COC)=[CH:4][S:5][CH:6]=1.Br>C(O)(=O)C>[Br:1][C:2]1[C:3]2=[CH:7][NH:8][C:9](=[O:17])[CH:10]=[C:4]2[S:5][CH:6]=1
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참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 66759489N-[(4-bromothiophen-3-yl)methyl]-2-ethoxy-3-methoxypropanamide

생성물 1

HCID 667597493-bromothieno[3,2-c]pyridin-6(5H)-one수율 45.2%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

A solution of N-[(4-bromothiophen-3-yl)methyl]-2-ethoxy-3-methoxypropanamide (729 mg, 2.26 mmol) in acetic acid (4.5 mL) and hydrogen bromide (2.2 mL, 41 mmol) was heated to reflux for 2 h. Upon cooling a precipitate formed. The precipitate was collected by vacuum filtration, washing with acetic acid (2×10 mL) and diethyl ether (2×10 mL). The collected solid was suspended in water (10 mL) and treated with solid sodium bicarbonate until the solution pH was −8. The solid was then collected by vacuum filtration, washing with water (2×10 mL). The collected solid was dried in an oven at 50° C. for 16 h to afford 235 mg (45%) of the title compound as a tan solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 11.82 (br. s., 1 H), 8.07 (s, 1 H), 7.55 (s, 1 H), 7.01 (s, 1H); MS (ESI): 230.01, 231.99 [M+H]+; HPLC tR=2.53 min (ZQ3, polar—4 min).

후처리

  1. temperatureto reflux for 2 h
  2. temperatureUpon cooling a precipitate
  3. customformed
  4. filtrationThe precipitate was collected by vacuum filtration
  5. washwashing with acetic acid (2×10 mL) and diethyl ether (2×10 mL)
  6. additiontreated with solid sodium bicarbonate until the solution pH was −8
  7. filtrationThe solid was then collected by vacuum filtration
  8. washwashing with water (2×10 mL)
  9. customThe collected solid was dried in an oven at 50° C. for 16 h

출처 및 근거

ORD 기록
ord-a1c405967eb2422a8def062f97e80263
출처 데이터셋
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08378104B2

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