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Dimethylformamide dimethyl acetal → N'-(4-cyclopropylmethoxy-2,5-dimethylphenyl)-N,N-dimethylformamidine

HRID 626305
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HRID 626305 반응식
[CH:1]1([CH2:4][O:5][C:6]2[C:11]([CH3:12])=[CH:10][C:9]([NH2:13])=[C:8]([CH3:14])[CH:7]=2)[CH2:3][CH2:2]1.CO[CH:17](OC)[N:18]([CH3:20])[CH3:19]>>[CH:1]1([CH2:4][O:5][C:6]2[C:11]([CH3:12])=[CH:10][C:9]([N:13]=[CH:17][N:18]([CH3:20])[CH3:19])=[C:8]([CH3:14])[CH:7]=2)[CH2:2][CH2:3]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 78373Dimethylformamide dimethyl acetalHCID 631807884-Cyclopropylmethoxy-2,5-dimethylphenylamine

생성물 1

HCID 117620572N'-(4-cyclopropylmethoxy-2,5-dimethylphenyl)-N,N-dimethylformamidine

실험 절차

A mixture of 0.23 g of 4-cyclopropylmethoxy-2,5-dimethylphenylamine and 10 mL of N,N-dimethylformamide dimethylacetal was stirred under heating and refluxing for 10 hours. The cooled reaction mixture was concentrated under reduced pressure. The resulting residue was subjected to silica gel column chromatography to obtain 0.18 g of N′-(4-cyclopropylmethoxy-2,5-dimethylphenyl)-N,N-dimethylformamidine (Compound of Present Invention (1-17)).

후처리

  1. temperatureunder heating
  2. temperaturerefluxing for 10 hours
  3. customThe cooled reaction mixture
  4. concentrationwas concentrated under reduced pressure
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출처 및 근거

ORD 기록
ord-52d86f6af6124df2b3592e6c4c6a8196
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09309191B2

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