HCID 86620957, compound → HCID 178422561, compound

HRID 1993886Notes

Reaction equation

HRID 1993886 reaction equation
[CH3:1][C:2]1[N:6]([C@@H:7]2[CH2:12][CH2:11][C@H:10]([NH2:13])[CH2:9][CH2:8]2)[C:5]2[CH:14]=[CH:15][C:16]([CH3:18])=[CH:17][C:4]=2[N:3]=1.[Cl:19][C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[CH2:25][CH:24]([CH:29]=O)[CH2:23]2>>[Cl:19][C:20]1[CH:21]=[C:22]2[C:26](=[CH:27][CH:28]=1)[CH2:25][CH:24]([CH2:29][NH:13][C@H:10]1[CH2:9][CH2:8][C@@H:7]([N:6]3[C:5]4[CH:14]=[CH:15][C:16]([CH3:18])=[CH:17][C:4]=4[N:3]=[C:2]3[CH3:1])[CH2:12][CH2:11]1)[CH2:23]2

Participants

3

Reactant 2

HCID 86620957HCID 86620957, compoundHCID 178422558HCID 178422558, compound

Product 1

HCID 178422561HCID 178422561, compound

Procedure

This compound was prepared from the hydrochloride salt of cis-4-(2,5-dimethyl-benzoimidazol-1-yl)-cyclohexylamine and 5-chloro-indan-2-carbaldehyde. 1H-NMR is consistent with the assigned structure, LC-MS showed a single peak, C25H30ClN3 (m/e) calcd 407.2128, obsd 408.2 (M+H).

Sources & evidence

ORD record
ord-3d5589dcd16d43c591a1c89fe66ef66a
Source dataset
uspto-grants-2010_01
Patent number
US07652053B2

Reaction notes

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