HuagongsheHuagongshe Chemistry Print Report · For research reference only
(1S,2R)-(+)-2-Amino-1-cyclopentanecarboxylic acid hydrochloride → (1S,2R)-2-[({4-[(2-methylquinolin-4-yl)methoxy]phenyl}sulfonyl)amino]cyclopentanecarboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (1S,2R)-(+)-2-Amino-1-cyclopentanecarboxylic acid hydrochloride | HCID 13831733 | — |
| Reactant | 4-(2-Methylquinolin-4-ylmethoxy)benzenesulfonyl chloride hydrochloride | HCID 86607865 | — |
| Product | (1S,2R)-2-[({4-[(2-methylquinolin-4-yl)methoxy]phenyl}sulfonyl)amino]cyclopentanecarboxylic acid | HCID 68817773 | 87.6% |
Reaction Steps
According to the procedure of Example 10, Step 1, the reaction of 141 mg (0.85 mmol) of (+)-(1S,2R)-2-amino-1-cyclopentane-carboxylic acid hydrochloride with 400 mg (1.04 mmol) of 4-(2-methyl-quinolin-4-ylmethoxy)-benzenesulfonyl chloride hydrochloride provided 327.9 mg of (1S,2R)-2-[({4-[(2-methylquinolin-4-yl)methoxy]phenyl}sulfonyl)amino]cyclopentanecarboxylic acid in 86% yield. MS: 441.1 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07595327B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-c4aac4bf89d3488ca27ebc61723e1a53 |
| Source note | uspto-grants-2009_09 |