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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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3-(5-Methyl-2-nitro-phenylamino)-hexanoic acid ethyl ester → 3-(2-Amino-5-methyl-phenylamino)-hexanoic acid ethyl ester

HRID 1747308
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인쇄 미리보기

반응식

HRID 1747308 반응식
[CH2:1]([O:3][C:4](=[O:21])[CH2:5][CH:6]([NH:10][C:11]1[CH:16]=[C:15]([CH3:17])[CH:14]=[CH:13][C:12]=1[N+:18]([O-])=O)[CH2:7][CH2:8][CH3:9])[CH3:2]>CO.[Pd]>[CH2:1]([O:3][C:4](=[O:21])[CH2:5][CH:6]([NH:10][C:11]1[CH:16]=[C:15]([CH3:17])[CH:14]=[CH:13][C:12]=1[NH2:18])[CH2:7][CH2:8][CH3:9])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 594976263-(5-Methyl-2-nitro-phenylamino)-hexanoic acid ethyl ester

생성물 1

HCID 594975033-(2-Amino-5-methyl-phenylamino)-hexanoic acid ethyl ester수율 110.3%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매2회

실험 절차

To a solution of 3-(5-Methyl-2-nitro-phenylamino)-hexanoic acid ethyl ester (1.4 g, 4.8 mmol) in MeOH (10 mL) was added a slurry of Pd/C (wet) (0.25 g) in MeOH. The reaction mixture was saturated with H2 balloon and stirred at room temperature for 2 h. When the reaction was complete, the reaction mixture was filtered through a pad of celite. The filtrate was concentrated to afford 1.4 g of the desired product as dark purplish oil. This product was used for the next reaction without further purification.

후처리

  1. filtrationthe reaction mixture was filtered through a pad of celite
  2. concentrationThe filtrate was concentrated

출처 및 근거

ORD 기록
ord-3faab4ed20c34003990e36cd07bb2b55
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09150556B2

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