HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl azetidine-3-carboxylate → HCID 57523797, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl azetidine-3-carboxylate | HCID 21717027 | — |
| Reactant | 2-Cyclopentyl-6-methoxyisonicotinic acid | HCID 58418037 | — |
| Reactant | HCID 178492428 | HCID 178492428 | — |
| Product | HCID 57523797 | HCID 57523797 | — |
Reaction Steps
The title compound is prepared starting from 2-cyclopentyl-6-methoxy-isonicotinic acid, 3-chloro-4-(2,2-dimethoxyethoxy)-N-hydroxy-5-methoxybenzimidamide and ethyl azetid ine-3-carboxylate in analogy to Example 43 and 1 (saponification); LC-MS: tR=0.88 min, [M+H]+=528.92; 1H NMR (CDCl3): δ 7.79 (d, J=1.5 Hz, 1H), 7.57 (d, J=1.4 Hz, 1H), 7.45 (s, 1H), 7.24 (s, 1H), 5.96 (s br, 1H), 4.55-4.64 (m, 2H), 4.44-4.54 (m, 2H), 4.32-4.38 (m, 2H), 4.00 (s, 6H), 3.65-3.74 (m, 1H), 3.58-3.65 (m, 2H), 3.18-3.27 (m, 1H), 2.05-2.14 (m, 2H), 1.82-1.94 (m, 4H), 1.75 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09133179B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-d18d771baff34523af4206453964acdb |
| Source note | uspto-grants-2015_09 |