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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Morpholine → (2-Amino-5-bromophenyl)(morpholino)methanone

HRID 1865604
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인쇄 미리보기

반응식

HRID 1865604 반응식
[Br:1][C:2]1[CH:13]=[C:6]2[C:7]([O:9]C(=O)[NH:11][C:5]2=[CH:4][CH:3]=1)=O.[NH:14]1[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1>C1COCC1>[NH2:11][C:5]1[CH:4]=[CH:3][C:2]([Br:1])=[CH:13][C:6]=1[C:7]([N:14]1[CH2:19][CH2:18][O:17][CH2:16][CH2:15]1)=[O:9]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8083MorpholineHCID 2885615-Bromoisatoic Anhydride

생성물 1

HCID 44448998(2-Amino-5-bromophenyl)(morpholino)methanone수율 94%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Into an 8 mL screw cap vial were added 5-bromoisatoic anhydride (0.200 g, 0.826 mmol), anhydrous THF (5 mL), and morpholine (101 mg, 1.16 mmol). The vial was sealed and placed in a heat block at 60° C. for 1.5 h after which it was concentrated under vacuum. The crude product was triturated with Et2O/hexanes to afford 111 mg (94%) of (2-Amino-5-bromo-phenyl)-morpholin-4-yl-methanone as a tan solid. m/z 285/287 [MH+].

후처리

  1. customInto an 8 mL screw cap vial
  2. customThe vial was sealed
  3. concentrationafter which it was concentrated under vacuum
  4. customThe crude product was triturated with Et2O/hexanes

출처 및 근거

ORD 기록
ord-469bb576991a45c4929bbe75bfd1aca7
출처 데이터셋
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07626021B2

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