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2,4-Dichloro-6-methylquinazoline → N-(3-Aminooxetan-3-ylmethyl)-2-chloro-6-methylquinazolin-4-amine

HRID 540191
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HRID 540191 반응식
[Cl:1][C:2]1[N:11]=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([CH3:13])[CH:8]=2)[N:3]=1.[NH2:14][CH2:15][C:16]1([NH2:20])[CH2:19][O:18][CH2:17]1>CO>[NH2:20][C:16]1([CH2:15][NH:14][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[C:7]([CH3:13])[CH:8]=3)[N:3]=[C:2]([Cl:1])[N:11]=2)[CH2:19][O:18][CH2:17]1
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참가 물질

4

반응물 2

HCID 142564832,4-Dichloro-6-methylquinazolineHCID 217130163-(Aminomethyl)oxetan-3-amine

생성물 1

HCID 86691401N-(3-Aminooxetan-3-ylmethyl)-2-chloro-6-methylquinazolin-4-amine

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 2,4-dichloro-6-methylquinazoline (645 mg, 3 mmol) and 3-(aminomethyl)oxetan-3-amine (340 mg, 3.3 mmol) in methanol (15 mL) was stirred at room temperature overnight. After the resulting mixture was concentrated in vacuo, the residue was purified by column chromatography (eluting with 10% methanol in dichloromethane) to afford the desired product.

후처리

  1. concentrationAfter the resulting mixture was concentrated in vacuo
  2. customthe residue was purified by column chromatography (eluting with 10% methanol in dichloromethane)

출처 및 근거

ORD 기록
ord-463f9b1bff4f4f8cb51f8be1b520ec80
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08871756B2

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