3-IODO-BENZAMIDINE → HCID 59254920, compound

HRID 2194994Notes

Reaction equation

HRID 2194994 reaction equation
[Cl:1]C1C=C(C=C(I)C=1)C(N)=N.FC1C=CC(I)=CC=1C(N)=N.IC1C=C(C=CC=1)C(N)=N.Cl[C:34]1[CH:35]=[C:36]([C:41]2[N:50]=[CH:49][C:48]3[CH2:47][CH2:46][C:45]4[N:51]=[C:52]([NH:54][C:55](=[O:57])[CH3:56])[S:53][C:44]=4[C:43]=3[N:42]=2)[CH:37]=[C:38]([I:40])[CH:39]=1.FC1C=CC(I)=CC=1C1N=CC2CCC3N=C(NC(=O)C)SC=3C=2N=1.IC1C=C(C2N=CC3CCC4N=C(NC(=O)C)SC=4C=3N=2)C=CC=1>>[Cl:1][C:35]1[CH:34]=[CH:39][C:38]([I:40])=[CH:37][C:36]=1[C:41]1[N:50]=[CH:49][C:48]2[CH2:47][CH2:46][C:45]3[N:51]=[C:52]([NH:54][C:55](=[O:57])[CH3:56])[S:53][C:44]=3[C:43]=2[N:42]=1

Participants

7

Reactant 6

HCID 35019453-IODO-BENZAMIDINEHCID 53417055HCID 53417055, compoundHCID 68601933HCID 68601933, compoundHCID 86615633HCID 86615633, compoundHCID 86615634HCID 86615634, compoundHCID 86615635HCID 86615635, compound

Product 1

HCID 59254920HCID 59254920, compound

Procedure

The following intermediates may be prepared analogously starting from 3-chloro-5-iodo-benzamidine, 2-fluoro-5-iodo-benzamidine and 3-iodo-benzamidine: N-[8-(3-chloro-5-iodo-phenyl)-4,5-dihydro-thiazolo[4,5-h]quinazolin-2-yl]-acetamide; N-[8-(2-fluoro-5-iodo-phenyl)-4,5-dihydro-thiazolo[4,5-h]quinazolin-2-yl]-acetamide; N-[8-(3-iodo-phenyl)-4,5-dihydro-thiazolo[4,5-h]quinazolin-2-yl]-acetamide

Workup

  1. customThe following intermediates may be prepared analogously

Sources & evidence

ORD record
ord-26499bf758284620be1105e41479edec
Source dataset
uspto-grants-2012_12
Patent number
US08334378B2

Reaction notes

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