HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Aminocyclohexanecarboxylic acid → HCID 66721057, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Aminocyclohexanecarboxylic acid | HCID 1366 | — |
| Reactant | HCID 66721121 | HCID 66721121 | — |
| Product | HCID 66721057 | HCID 66721057 | 96.3% |
Reaction Steps
According to the saponification/peptide coupling steps described in examples 1.7 and 1.8 respectively, starting from 1.8 g (3.62 mmol) of methyl 3,5-dichloro-2′-{4-chloro-3-[3-(dimethylamino)propoxy]phenyl}-2,3′-bipyridine-6′-carboxylate and 472 mg (3.3 mmol) of 2-aminocyclohexane-2-carboxylic acid, we obtain 1.12 g of 1-{[(3,5-dichloro-2′-{4-chloro-3-[3-(dimethylamino)propoxy]phenyl}-2,3′-bipyridin-6′-yl)carbonyl]amino}cyclohexanecarboxylic acid hydrochloride in the form of white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08552201B2 |
| Source dataset | uspto-grants-2013_10 |
| ORD ID | ord-b726ac18fb164b668b312e1397808eb9 |
| Source note | uspto-grants-2013_10 |