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Acetic Acid → 2-[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]ethanamine acetate

HRID 2100684
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반응식

HRID 2100684 반응식
[Cl:1][C:2]1[C:3]([CH2:12][C:13]#[N:14])=[N:4][CH:5]=[C:6]([C:8]([F:11])([F:10])[F:9])[CH:7]=1.[C:15]([OH:18])(=[O:17])[CH3:16]>[Pd]>[C:15]([OH:18])(=[O:17])[CH3:16].[Cl:1][C:2]1[C:3]([CH2:12][CH2:13][NH2:14])=[N:4][CH:5]=[C:6]([C:8]([F:11])([F:9])[F:10])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 176Acetic AcidHCID 162272722-[3-Chloro-5-(trifluoromethyl)pyridin-2-yl]acetonitrile2회

생성물 1

HCID 690470172-[3-Chloro-5-(trifluoromethyl)-2-pyridinyl]ethanamine acetate

시약·촉매·용매 1

HCID 23938Palladium촉매

실험 절차

113 g of [3-chloro-5-(trifluoromethyl)-2-pyridinyl]acetonitrile (0.51 mol, 1 eq.) are diluted in 2.5 L of acetic acid. 30 g of palladium (5% on charcoal) are added. The reaction medium is stirred at ambient temperature under a hydrogen pressure of 5 bar. The progress of the reaction is followed by TLC; when the [3-chloro-5-(trifluoromethyl)-2-pyridinyl]acetonitrile has been completely used up, the medium is filtered over a bed of celite, and then concentrated to dryness so as to produce the 2-[3-chloro-5-(trifluoromethyl)-2-pyridinyl]ethanamine acetate.

후처리

  1. filtrationthe medium is filtered over a bed of celite
  2. concentrationconcentrated to dryness so as

출처 및 근거

ORD 기록
ord-50ff42d905544e00b2130beb9d36a904
출처 데이터셋
uspto-grants-2009_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07572818B2

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