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Water → (R)-2-(5-bromo-4-cyano-2-fluorophenylamino)-2-cyclopropylacetamide

HRID 84870
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HRID 84870 반응식
[Br:1][C:2]1[CH:9]=[C:8](F)[C:7]([F:11])=[CH:6][C:3]=1[C:4]#[N:5].Cl.[NH2:13][C@H:14]([CH:18]1[CH2:20][CH2:19]1)[C:15]([NH2:17])=[O:16].CCN(C(C)C)C(C)C.O>CS(C)=O.CCOC(C)=O>[Br:1][C:2]1[C:3]([C:4]#[N:5])=[CH:6][C:7]([F:11])=[C:8]([NH:13][C@H:14]([CH:18]2[CH2:20][CH2:19]2)[C:15]([NH2:17])=[O:16])[CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 81531DiisopropylethylamineHCID 192612772-Bromo-4,5-difluorobenzonitrileHCID 67508384(R)-2-amino-2-cyclopropylacetamide hydrochloride

생성물 1

HCID 67509451(R)-2-(5-bromo-4-cyano-2-fluorophenylamino)-2-cyclopropylacetamide수율 80.9%

시약·촉매·용매 2

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
HCID 679
Dimethyl Sulfoxide
용매
HCID 8857Ethyl Acetate용매

실험 절차

A solution of 2-bromo-4,5-difluorobenzonitrile (170 mg, 0.780 mmol), (R)-2-amino-2-cyclopropylacetamide hydrochloride (120 mg, 0.797 mmol) and DIEA (0.500 mL, 2.87 mmol) in DMSO (3 mL) was stirred at 120 C for 18 h. Water and EtOAc were added. The organic phase was separated, dried over Na2SO4, concentrated in vacuo to give (R)-2-(5-bromo-4-cyano-2-fluorophenylamino)-2-cyclopropylacetamide (197 mg)

후처리

  1. customThe organic phase was separated
  2. dry with materialdried over Na2SO4
  3. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-0cf96488ca134f8e8d3f88641319d7a5
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846928B2

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