HCID 20362426, compound → HCID 20362403, compound

HRID 1679305Notes

Reaction equation

HRID 1679305 reaction equation
[Cl-].[CH2:2]([C:5]1[S:9][CH:8]2[N:10]([CH2:13][C:14]3[CH:19]=[CH:18][C:17](F)=[CH:16][CH:15]=3)[CH:11]=[CH:12][N+:7]2([CH2:21][CH3:22])[C:6]=1[CH2:23][CH3:24])CC.[Cl-].C(C1SC2N(CC3C=CC(F)=CC=3)C=C[N+]=2C=1)(C)C.[Br-].C1(C2[N+]3C=CN(CC4C=CC=CC=4OC)C=3SC=2)C=CC=CC=1.[Cl-].COC1C=C(C=C(OC)C=1)CC1[N+]2C=CN(CC3C=CC=CC=3)C=2SC=1.[Br-].CC1[N+]2C=CN(CC3C=CC(C4C=CC=CC=4)=CC=3)C=2SC=1.[Br-].CC1C=C(C)C=CC=1CC1[N+]2C=C(C)N(CC3C=CC([Cl:140])=CC=3)C=2SC=1.[Br-].ClC1C=CC(C2[N+]3C=CN(CC#C)C=3SC=2)=CC=1.[Cl-].CC1C=C(C)C=CC=1C1[N+]2C=C(C3C=CC(C)=CC=3C)N(CC3C=CC=CC=3)C=2SC=1.[Cl-].FC1C=CC(C[N+]2C=CN3C4CCCCC=4SC=23)=CC=1.[Br-].C([N+]1C=CN2C3CCCCC=3SC=12)C#C>>[Cl-:140].[CH3:2][C:5]1[S:9][CH:8]2[N:10]([CH2:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=3)[CH:11]=[CH:12][N+:7]2([CH2:21][CH3:22])[C:6]=1[CH2:23][CH3:24]

Participants

11

Procedure

2-n-propyl-3,4-diethyl-7-(p-fluorobenzyl)imidazo[2,1-b]thiazolium chloride, 2-i-propyl-7-(p-fluorobenzyl)imidazo[2,1-b]thiazolium chloride; 3-phenyl-7-(o-methoxybenzyl)imidazo[2,1-b]thiazolium bromide; 3-adamantyl-6-phenyl-7-(m-trifluorobenzyl)imidazo[2,1-b]thiazolium bromide; 3-(3,5-dimethoxybenzyl)-7-benzylimidazo[2,1-b]thiazolium chloride, 3-methyl-7-(p-phenylbenzyl)imidazo[2,1-b]thiazolium bromide; 3-(2,4-dimethylbenzyl)-6-methyl-7-(p-chlorobenzyl)imidazo[2,1-b]thiazolium bromide; 3-(p-chlorophenyl)-7-propargylimidazo[2,1-b]thiazolium bromide; 3,6-bis(2,4-dimethylphenyl)-7-benzylimidazo[2,1-b]thiazolium chloride; 1-(p-fluorobenzyl-5,6,7,8-tetrahydroimidazo[2,1-b]benzthiazolium chloride and 1-propargyl-5,6,7,8-tetrahydroimidazo[2,1-b]benzthiazolium bromide.

Sources & evidence

ORD record
ord-dbff6f3a53d8421bb10472c633fe045c
Source dataset
uspto-grants-1978_03
Patent number
US04080339

Reaction notes

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