HCID 59323909, compound → HCID 59323904, compound

Reaction equation

C(=[N:14][C:15]1[S:16][C:17]([C:21]2[CH:26]=[CH:25][C:24]([N:27]3[CH:31]=[CH:30][CH:29]=[N:28]3)=[CH:23][CH:22]=2)=[C:18]([CH3:20])[N:19]=1)(C1C=CC=CC=1)C1C=CC=CC=1.NC1SC(C2C=CC(C(=O)C)=CC=2)=C(C)N=1>>[CH3:20][C:18]1[N:19]=[C:15]([NH2:14])[S:16][C:17]=1[C:21]1[CH:26]=[CH:25][C:24]([N:27]2[CH:31]=[CH:30][CH:29]=[N:28]2)=[CH:23][CH:22]=1

Participants

Reactant 2

HCID 59323909HCID 59323909, compound

HCID 59383111HCID 59383111, compound

Product 1

HCID 59323904HCID 59323904, compound

Procedure

This compound is prepared from benzhydrylidene-[4-methyl-5-(4-pyrazol-1-yl-phenyl)-thiazol-2-yl]-amine analogously to 1-[4-(2-amino-4-methyl-thiazol-5-yl)-phenyl]-ethanone (Intermediate A1 step 4).

Sources & evidence

ORD record: ord-3a31cc4a26cf4342b9b4ab574df12af2
Source dataset: uspto-grants-2010_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07799810B2

Reaction notes

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