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1-Chloro-N,N-2-trimethylpropenylamine → 2-[chloro-(4-cyano-phenyl)-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl ester

HRID 2204307
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HRID 2204307 반응식
[Cl:1]C(N(C)C)=C(C)C.[CH2:9]([O:11][C:12]([C:14]1[CH:18]=[CH:17][N:16]([CH:19]([CH3:21])[CH3:20])[C:15]=1[CH:22]([C:24]1[CH:29]=[CH:28][C:27]([C:30]#[N:31])=[CH:26][CH:25]=1)O)=[O:13])[CH3:10]>C(Cl)Cl>[CH2:9]([O:11][C:12]([C:14]1[CH:18]=[CH:17][N:16]([CH:19]([CH3:21])[CH3:20])[C:15]=1[CH:22]([Cl:1])[C:24]1[CH:29]=[CH:28][C:27]([C:30]#[N:31])=[CH:26][CH:25]=1)=[O:13])[CH3:10]
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참가 물질

4

반응물 2

HCID 6407921-Chloro-N,N-2-trimethylpropenylamineHCID 867031112-[(4-cyano-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl ester

생성물 1

HCID 867031102-[chloro-(4-cyano-phenyl)-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl ester

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

1-Chloro-N,N,2-trimethylpropenylamine [26189-59-3] (4.80 mmol) was added to a solution of 2-[(4-cyano-phenyl)-hydroxy-methyl]-1-isopropyl-1H-pyrrole-3-carboxylic acid ethyl ester (Step H4) (3.20 mmol) in CH2Cl2 (15 mL) and the mixture was stirred at rt for 2.5 h. CH2Cl2 was added and the reaction mixture was concentrated to dryness (2×) to afford the title compound as a yellow-orange oil. tR: 5.71 min (sample in MeOH) (HPLC 4); ESI-MS: tR=1.26 min (LC-MS 1).

후처리

  1. concentrationthe reaction mixture was concentrated to dryness (2×)

출처 및 근거

ORD 기록
ord-8906da3d00bf4f29801e301008aa88e6
출처 데이터셋
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09365576B2

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