HCID 58294505, compound → HCID 178519354, compound

HRID 2360937Notes

Reaction equation

HRID 2360937 reaction equation
[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([OH:12])=O)=[CH:9][C:4]=2[N:3]=[CH:2]1.[O:13]1[CH:17]=[CH:16][C:15]([C:18]2[CH:19]=[CH:20][C:21]3[CH2:22][C@H:23]4[C@@H:28]([C:29]=3[CH:30]=2)[CH2:27][CH2:26][CH2:25][NH:24]4)=[CH:14]1>>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([N:24]3[CH2:25][CH2:26][CH2:27][C@@H:28]4[C:29]5[CH:30]=[C:18]([C:15]6[CH:16]=[CH:17][O:13][CH:14]=6)[CH:19]=[CH:20][C:21]=5[CH2:22][C@H:23]34)=[O:12])=[CH:9][C:4]=2[N:3]=[CH:2]1

Participants

3

Reactant 2

HCID 58294505HCID 58294505, compoundHCID 178524171HCID 178524171, compound

Product 1

HCID 178519354HCID 178519354, compoundYield 14%

Procedure

The title compound is prepared from 1H-benzoimidazole-5-carboxylic acid and cis-6-furan-3-yl-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine following a procedure analogous to that described in Example 1. Yield: 14% of theory; LC (method 1): tR=2.89 min; Mass spectrum (ESI+): m/z=384 [M+H]+.

Sources & evidence

ORD record
ord-cc47d4a78b5745b799378b12d6116bfe
Source dataset
uspto-grants-2014_04
Patent number
US08686149B2

Reaction notes

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