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2-Methyl-4-nitrophenyl isothiocyanate → HCID 178428743, 화합물

HRID 276541
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HRID 276541 반응식
[Cl-].[CH3:2][C:3]([NH3+:7])([CH3:6])[CH2:4]Cl.[CH3:8][C:9]1[CH:14]=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:11][C:10]=1[N:18]=[C:19]=[S:20]>>[CH3:8][C:9]1[CH:14]=[C:13]([N+:15]([O-:17])=[O:16])[CH:12]=[CH:11][C:10]=1[N:18]=[C:19]1[NH:7][C:3]([CH3:6])([CH3:2])[CH2:4][S:20]1
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참가 물질

3

반응물 2

HCID 1456212-Methyl-4-nitrophenyl isothiocyanateHCID 865901841,1-Dimethyl-2-chloroethylammonium chloride2회

생성물 1

HCID 178428743HCID 178428743, 화합물

실험 절차

1,1-Dimethyl-2-hydroxyamine was converted to 1,1-dimethyl-2-chloroethylammonium chloride according to Method B7a. 2-Methyl-4-nitrophenyl isothiocyanate was reacted with 1,1-dimethyl-2-chloroethylammonium chloride according to Method C1a to give 2-(2-methyl-4-nitrophenylimino)-4,4-dimethyl-1,3-thiazolidine. The thiazolidine was reacted with 2-methylprop-2-en-1-yl bromide according to Method D2g to afford 2-(2-methyl-4-nitrophenylimino)-4,4-dimethyl-3-(2-methylprop-2-en-1-yl)-1,3-thiazolidine HBr salt.

출처 및 근거

ORD 기록
ord-c56d86f8a875493e8df7279988412b51
출처 데이터셋
uspto-grants-2002_03
DOI
10.6084/m9.figshare.5104873.v1
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특허 번호
US06353006B1

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