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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12209Generated: October 29, 2026

HCID 67165900, compound → cis-2-amino-cyclopentanecarboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amide

https://huagongshe.com/reaction/12209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67165900HCID 67165900—
SolventTrifluoroacetic acidHCID 6422—
Productcis-2-amino-cyclopentanecarboxylic acid (6-chloro-9H-beta-carbolin-8-yl)-amideHCID 11393321106.1%

Reaction Steps

A solution of 2-(tert-butoxycarbonylamino)-cyclopentanecarboxylic acid (6-chloro-9H-β-carbolin-8-yl) amide (736 mg, 1.72 mmol) in trifluoroacetic acid (5 ml) was stirred at RT for 20 min, then concentrated to an orange oil. The oil was dissolved in MeOH (5 ml) and neutralized with a saturated aqueous sodium bicarbonate solution (25 ml). The resulting mixture was further diluted with H2O (25 ml) and EtOAc (100 ml). The aqueous layer was removed and extracted with EtOAc (100 ml). The organic layers were combined, washed with brine, dried over MgSO4, filtered and concentrated to yellow solids (507 mg). These solids were dissolved in MeOH (5 ml) and a solution of HCl in dioxane (4 M, 1.5 ml) was added. The bright yellow solution was stirred 30 min, then concentrated to yield cis-2-amino-cyclopentanecarboxylic acid (6-chloro-9H-β-carbolin-8-yl)-amide as a yellow powder (600 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727985B2
Source datasetuspto-grants-2010_06
ORD IDord-d432fcaf3af3447bbf3a4599b44cc9a3
Source noteuspto-grants-2010_06