(R)-5-bromo-indan-2-carbaldehyde → HCID 178458921, compound

HRID 1993897Notes

Reaction equation

HRID 1993897 reaction equation
[NH2:1][C@@H:2]1[CH2:7][CH2:6][C@H:5]([N:8]2[C:12]3[CH:13]=[CH:14][C:15]([Cl:17])=[CH:16][C:11]=3[N:10]=[C:9]2[C:18]([OH:21])([CH3:20])[CH3:19])[CH2:4][CH2:3]1.[Br:22][C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[CH2:28][C@@H:27]([CH:32]=O)[CH2:26]2>>[Br:22][C:23]1[CH:24]=[C:25]2[C:29](=[CH:30][CH:31]=1)[CH2:28][C@@H:27]([CH2:32][NH:1][C@@H:2]1[CH2:3][CH2:4][C@H:5]([N:8]3[C:12]4[CH:13]=[CH:14][C:15]([Cl:17])=[CH:16][C:11]=4[N:10]=[C:9]3[C:18]([OH:21])([CH3:19])[CH3:20])[CH2:6][CH2:7]1)[CH2:26]2

Participants

3

Reactant 2

HCID 86620959(R)-5-bromo-indan-2-carbaldehydeHCID 178458917HCID 178458917, compound

Product 1

HCID 178458921HCID 178458921, compound

Procedure

This compound was prepared from the hydrochloride salt of cis-2-[1-(4-amino-cyclohexyl)-5-chloro-1H-benzoimidazol-2-yl]-propan-2-ol and (R)-5-bromo-indan-2-carbaldehyde. 1H-NMR is consistent with the assigned structure, LC-MS showed a single peak, C26H31BrClN3O (m/e) calcd 515.1339, obsd 516.2 (M+H).

Sources & evidence

ORD record
ord-a3c15408ef534da99a0bab01d83c4293
Source dataset
uspto-grants-2010_01
Patent number
US07652053B2

Reaction notes

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