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Water → 2-Bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine

HRID 84466
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HRID 84466 반응식
[Br:1]N1C(=O)CCC1=O.[S:9]1[C:13]2[C:14]3[CH:22]=[N:21][CH:20]=[CH:19][C:15]=3[O:16][CH2:17][CH2:18][C:12]=2[CH:11]=[CH:10]1.O>CN(C)C=O>[Br:1][C:10]1[S:9][C:13]2[C:14]3[CH:22]=[N:21][CH:20]=[CH:19][C:15]=3[O:16][CH2:17][CH2:18][C:12]=2[CH:11]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 67184N-bromobutanimideHCID 579001994,5-Dihydropyrido[4,3-b]thieno[2,3-d]oxepine

생성물 1

HCID 579000912-Bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine수율 65.4%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매2회

실험 절차

N-Bromosuccinimide (0.237 g, 1.33 mmol) in dimethylformamide (4 mL) was added dropwise to a solution of 4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine (0.250 g, 1.23 mmol) in dimethylformamide (4 mL, 100 mmol) at 0° C. The reaction mixture was stirred for 18 hours at room temperature. The reaction mixture was mixed with 40 ml of water and extracted with 20 ml of ethylacetate twice. Combined organic extracts were washed with water and brine, and dried over MgSO4. The solvent was evaporated affording 2-bromo-4,5-dihydropyrido[4,3-b]thieno[2,3-d]oxepine (0.227 g, 63%). 1H NMR (500 MHz, CDCl3) 8.76 (s, 1H), 8.26 (d, J=5.4, 1H), 6.90 (d, J=5.5, 1H), 6.88 (s, 1H), 4.36 (t, J=4.7, 2H), 3.19 (t, J=4.8, 2H). MS (ESI+) 282.0

후처리

  1. extractionextracted with 20 ml of ethylacetate twice
  2. washCombined organic extracts were washed with water and brine
  3. dry with materialdried over MgSO4
  4. customThe solvent was evaporated

출처 및 근거

ORD 기록
ord-213476a895a04bf08c0233c3f51e62c8
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846762B2

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