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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Butanoic acid, 2-bromo-, ethyl ester → 8-bromo-2-ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one

HRID 76341
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HRID 76341 반응식
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([NH2:8])[C:3]=1[OH:9].N12CCCN=C1CCCCC2.[CH3:21][CH2:22][CH:23](Br)[C:24](OCC)=[O:25]>CN1CCCC1=O>[Br:1][C:2]1[C:3]2[O:9][CH:23]([CH2:22][CH3:21])[C:24](=[O:25])[NH:8][C:4]=2[CH:5]=[CH:6][CH:7]=1
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참가 물질

5

반응물 3

HCID 79039Butanoic acid, 2-bromo-, ethyl esterHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 155315062-Amino-6-bromophenol

생성물 1

HCID 667152308-bromo-2-ethyl-2H-benzo[b][1,4]oxazin-3(4H)-one수율 71%

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매

실험 절차

Procedure & NMR Data: 1.5 g (7.9 mmol) of 2-bromo-6-aminophenol, 1.08 ml (0.9 eq, 7.11 mmol) of 1.8-diazabicyclo[5.4.0]undec-7-ene and 3.5 mL of DL-Ethyl 2-bromobutyrate (3 eq, 23.7 mmol)) in 30 mL of 1-Methyl-2-pyrrolidinone were mixed. 1.447 g of P1 were obtained, yield 71%.

후처리

  1. custom1.447 g of P1 were obtained

출처 및 근거

ORD 기록
ord-efd9c31ad02147a0b0605978b604591c
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835628B2

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