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Pyridine → Phenyl (6-methoxypyrazin-2-yl)carbamate

HRID 1666357
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인쇄 미리보기

반응식

HRID 1666357 반응식
[NH2:1][C:2]1[CH:7]=[N:6][CH:5]=[C:4]([O:8][CH3:9])[N:3]=1.CC#N.N1C=CC=CC=1.[C:19]1([O:25][C:26](Cl)=[O:27])[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C1COCC1>[CH3:9][O:8][C:4]1[N:3]=[C:2]([NH:1][C:26](=[O:27])[O:25][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)[CH:7]=[N:6][CH:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 1049PyridineHCID 6342AcetonitrileHCID 15891Phenyl chloroformateHCID 48681936-Methoxypyrazin-2-amine

생성물 1

HCID 66875760Phenyl (6-methoxypyrazin-2-yl)carbamate

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

실험 절차

2-Amino-6-methoxy-pyrazine (1.00 g, 8 mmol) was dissolved in a mix of 1:2 THF:MeCN (30 mL), cooled to 0° C., and treated with pyridine (0.664 g, 8.3 mmol) followed by the dropwise addition of phenylchloroformate (1.3 g, 8.3 mmol) in THF (10 mL). After stirring for 18 h, the resulting white solid was collected by filtration (1.3 g, 68%) and was used without further purification.

후처리

  1. filtrationthe resulting white solid was collected by filtration (1.3 g, 68%)
  2. customwas used without further purification

출처 및 근거

ORD 기록
ord-b1d53a37aed0422eaba5b63a3da91fa7
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044052B2

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