cis-7-Nitro-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridin-6-ol → HCID 178519369, compound

HRID 2360944Notes

Reaction equation

HRID 2360944 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.[N+:13]([C:16]1[C:28]([OH:29])=[CH:27][C:26]2[C@@H:25]3[C@@H:20]([NH:21][CH2:22][CH2:23][CH2:24]3)[CH2:19][C:18]=2[CH:17]=1)([O-:15])=[O:14]>>[NH:1]1[C:5]2[CH:6]=[CH:7][C:8]([C:10]([N:21]3[CH2:22][CH2:23][CH2:24][C@@H:25]4[C:26]5[CH:27]=[C:28]([OH:29])[C:16]([N+:13]([O-:15])=[O:14])=[CH:17][C:18]=5[CH2:19][C@H:20]34)=[O:12])=[CH:9][C:4]=2[N:3]=[CH:2]1

Participants

3

Reactant 2

HCID 58294503cis-7-Nitro-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridin-6-olHCID 178524171HCID 178524171, compound

Product 1

HCID 178519369HCID 178519369, compoundYield 32%

Procedure

The title compound is prepared from 1H-benzoimidazole-5-carboxylic acid and cis-7-nitro-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridin-6-ol following a procedure analogous to that described in Example 1. Yield: 32% of theory; LC (method 1): tR=2.43 min; Mass spectrum (ESI+): m/z=379 [M+H]+.

Sources & evidence

ORD record
ord-862ce6591e6146a3a9bb4ee200e519ea
Source dataset
uspto-grants-2014_04
Patent number
US08686149B2

Reaction notes

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