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Sodium → 7-Bromo-4,5-dihydro-1H-benzo[b][1,4]diazepin-2(3H)-one

HRID 1485384
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HRID 1485384 반응식
[Na].[NH2:2][C:3]1[CH:8]=[CH:7][C:6]([Br:9])=[CH:5][C:4]=1[NH:10][CH2:11][CH2:12][C:13]([O:15]C)=O>CO>[Br:9][C:6]1[CH:7]=[CH:8][C:3]2[NH:2][C:13](=[O:15])[CH2:12][CH2:11][NH:10][C:4]=2[CH:5]=1
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참가 물질

4

반응물 2

HCID 5360545SodiumHCID 65343583HCID 65343583, 화합물

생성물 1

HCID 105380607-Bromo-4,5-dihydro-1H-benzo[b][1,4]diazepin-2(3H)-one수율 24%

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

Sodium (2.4 g, 104 mmol) was added in portions to 50 mL of methanol until it dissolved. The solution was then added dropwise to a cooled solution of methyl 3-((2-amino-5-bromophenyl)amino)propanoate (9.4 g, 34.6 mmol) in 50 mL of methanol at 0° C. After additional, the mixture was stirred at room temperature overnight. It was concentrated, added with water (50 mL), extracted with ethyl acetate (50 mL) and purified by CombiFlash (PE:EA=5:1) to give 7-bromo-4,5-dihydro-1H-benzo[b][1,4]diazepin-2(3H)-one (2 g, yield 24%). LRMS (M+H)+: 240 m/z. 1H NMR (300 MHz, CDCl3) δ 2.68-2.72 (t, J=6.0 Hz, 2H), 3.68-3.72 (t, J=6.0 Hz, 2H), 6.79-6.82 (d, J=8.7 Hz, 2H), 6.98-7.06 (m, 2H), 8.00 (br, 1H).

후처리

  1. dissolutiondissolved
  2. concentrationIt was concentrated
  3. additionadded with water (50 mL)
  4. extractionextracted with ethyl acetate (50 mL)
  5. custompurified by CombiFlash (PE:EA=5:1)

출처 및 근거

ORD 기록
ord-f4506d049d724f91b764d6c5485230bb
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09422292B2

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