HCID 16237421、化合物 → HCID 66830863、化合物

反応式

[Br-:1].[C:2]([CH:5]([CH2:29][CH2:30]C)[CH2:6][CH2:7][N:8]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[S:10][C:9]1=[CH:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[N+:21]([CH3:28])=[CH:20][CH:19]=1)([OH:4])=[O:3].[Br-].C(C(CC)CCC[N+]1C2C=CC=CC=2SC=1C)(O)=O.[Br-].CC1SC2C=CC=CC=2[NH+]=1.[Br-].C[N+]1C2C(=CC=CC=2)C(C=C2N(CCCCC(O)=O)C3C=CC=CC=3S2)=CC=1>>[Br-:1].[C:2]([CH:5]([CH2:29][CH3:30])[CH2:6][CH2:7][N:8]1[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=2[S:10][C:9]1=[CH:17][C:18]1[C:27]2[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=2)[N+:21]([CH3:28])=[CH:20][CH:19]=1)([OH:4])=[O:3]

参加物

反応物 4

HCID 16237421HCID 16237421、化合物

HCID 66830866HCID 66830866、化合物

HCID 66830876HCID 66830876、化合物

HCID 66830885HCID 66830885、化合物

生成物 1

HCID 66830863HCID 66830863、化合物収率 22%

実験手順

Furthermore, 4-((3-(3-carboxyhexyl)benzo[d]thiazole-2(3H)-ylidene) methyl)-1-methylquinoliniumbromide with a linker (a polymethylene chain linked to a carboxyl group) having a carbon number n of 6 was synthesized from the mixture of 3-(4-carboxyhexyl)-2-methylbenzothiazolium bromide and 2-methylbenzothiazolium bromide by the same method as that used for Compound 107, which was obtained with a yield of 22%. The instrumental analytical values are indicated below.