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Triethylamine → 3-{3-[(6-Nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}acrylonitrile

HRID 712039
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인쇄 미리보기

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HRID 712039 반응식
Cl.[NH2:2][CH:3]1[CH2:8][CH2:7][CH2:6][CH:5]([CH:9]=[CH:10][C:11]#[N:12])[CH2:4]1.Cl[C:14]1[C:19]([N+:20]([O-:22])=[O:21])=[CH:18][N:17]=[C:16]2[CH:23]=[CH:24][S:25][C:15]=12.C(N(CC)CC)C>C(O)(C)C>[N+:20]([C:19]1[C:14]([NH:2][CH:3]2[CH2:8][CH2:7][CH2:6][CH:5]([CH:9]=[CH:10][C:11]#[N:12])[CH2:4]2)=[C:15]2[S:25][CH:24]=[CH:23][C:16]2=[N:17][CH:18]=1)([O-:22])=[O:21]
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참가 물질

5

반응물 3

HCID 8471TriethylamineHCID 142079507-Chloro-6-nitrothieno[3,2-b]pyridineHCID 867174923-(3-Aminocyclohexyl)acrylonitrile hydrochloride

생성물 1

HCID 867174943-{3-[(6-Nitrothieno[3,2-b]pyridin-7-yl)amino]cyclohexyl}acrylonitrile

시약·촉매·용매 1

HCID 3776Isopropanol용매

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온도
90 °C

실험 절차

A mixture of 3-(3-aminocyclohexyl)acrylonitrile hydrochloride (0.090 g, 0.48 mmol), 7-chloro-6-nitrothieno[3,2-b]pyridine (0.085 g, 0.40 mmol) and triethylamine (0.22 mL, 1.6 mmol) in isopropyl alcohol (0.9 mL) was heated at 90° C. for 1 h. The mixture was concentrated to give the desired product to be used in the next step directly. LCMS calculated for C16H17N4O2 (M+H)+: m/z=329.1. Found: 329.1.

후처리

  1. concentrationThe mixture was concentrated

출처 및 근거

ORD 기록
ord-4f1ad327ffbd42b096cbbb49504c482e
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09181271B2

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