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Thionyl Chloride → HCID 59561810, 화합물

HRID 896341
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HRID 896341 반응식
[C:1]([O:5][C:6](=[O:25])[NH:7][CH2:8][C:9]1[CH:24]=[CH:23][C:12]2[N:13]([CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])[C:14]([CH2:16]O)=[N:15][C:11]=2[CH:10]=1)([CH3:4])([CH3:3])[CH3:2].S(Cl)([Cl:28])=O>C(Cl)Cl>[C:1]([O:5][C:6](=[O:25])[NH:7][CH2:8][C:9]1[CH:24]=[CH:23][C:12]2[N:13]([CH2:18][CH2:19][CH:20]([CH3:22])[CH3:21])[C:14]([CH2:16][Cl:28])=[N:15][C:11]=2[CH:10]=1)([CH3:4])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 59561849tert-Butyl N-[[2-(hydroxymethyl)-1-isopentyl-benzimidazol-5-yl]methyl]-carbamate

생성물 1

HCID 59561810HCID 59561810, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

반응 조건

온도
0 °C

실험 절차

To a cooled (0° C.) solution of [2-hydroxymethyl-1-(3-methyl-butyl)-1H-benzoimidazol-5-ylmethyl]-carbamic acid tert-butyl ester (146 mg, 0.42 mmol) in DCM (5 mL) was added thionyl chloride (46 μL, 0.63 mmol). The solution was stirred at 0° C. for 15 min. and concentrated in vacuo to give [2-chloromethyl-1-(3-methyl-butyl)-1H-benzoimidazol-5-ylmethyl]-carbamic acid tert-butyl ester; HCl salt (176 mg, 100%) as a white solid, which was used without further purification.

후처리

  1. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-b2c49bbd95524e73ad2d24378976c321
출처 데이터셋
uspto-grants-2005_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06919331B2

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