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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521041Generated: October 30, 2026

HCID 10798140, compound → HCID 178421263, compound

https://huagongshe.com/reaction/521041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10798140HCID 10798140—
ReactantHCID 67201248HCID 67201248—
ReactantHCID 178524171HCID 178524171—
ProductHCID 178421263HCID 17842126320%

Reaction Steps

The title compound is prepared from 1H-benzoimidazole-5-carboxylic acid and an isomeric mixture of cis-10b-methyl-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline and trans-10b-methyl-1,2,3,4,4a,5,6,10b-octahydro-benzo[f]quinoline following a procedure analogous to that described in Example 1 yielding a mixture of Example 10 and Example 11 which is separated by HPLC on reversed phase (MeOH/H2O/NH4OH). Yield: 20% of theory; LC (method 2): tR=3.40 min; Mass spectrum (ESI+): m/z=346 [M+H]+; 1H NMR (400 MHz, DMSO-d6, mixture of 2 rotamers) δ 1.33 (s, 3H), 1.42-1.53 (m, 2H), 1.62-1.78 (m, 1H), 2.15-2.23 (m, 1H), 2.27-2.35 (m, 1H), 2.75-2.90 (m, 3H), 3.07-3.18 (m, 1H), 3.43-3.49 (m, 1H), 3.69-3.77 (m, 1H), 7.04-7.18 (m, 3H), 7.20-7.34 (m, 2H), 7.56 (broad s, 0.75H), 7.58 (broad s, 0.25H), 7.67 (broad s, 0.75H), 7.69 (broad s, 0.25H), 8.29 (s, 1H), 12.53-12.62 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328072B2
Source datasetuspto-grants-2016_05
ORD IDord-88c2b03b887c4290821afbe2f1afdba1
Source noteuspto-grants-2016_05