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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1479109Generated: November 3, 2026

Piperidine → HCID 131736565, compound

https://huagongshe.com/reaction/1479109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 131736566HCID 131736566—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 131736565HCID 131736565214.7%

Reaction Steps

Piperidine (0.4 mL) was added to a solution of 7-[2-(6-chloro-5,7-dimethyl-1H,3H-2,4,7a,8-tetraaza-cyclopenta[a]indene-2-carbonyl)-benzyl]-3-oxa-7,9-diaza-bicyclo[3.3.1]nonane-9-carboxylic acid 9H-fluoren-9-ylmethyl ester (354 mg, 0.44 mmol) in DMF (4 mL). The resulting mixture was stirred at RT for 30 min, then diluted with water (20 mL). The precipitate was filtered off and washed with water (2×). After purification by flash chromatography (silica, DCM/EtOH/28% aqueous ammonia), the parent compound was dissolved in water (8 ml) and the solution was lyophilized to give the title compound as a yellow solid (170 mg, 72%). 1H NMR (300 MHz, DMSO-d6) δ 10.92 (br s, 2H), 10.01 (br s, 1H), 7.95-7.78 (m, 2H), 7.72-7.60 (m, 2H), 5.01 (s, 1H), 4.99 (s, 1H), 4.85 (s, 1H), 4.80 (s, 1H), 4.46 (s, 2H), 4.19-4.04 (m, 4H), 3.97-3.70 (m, 6H), 2.86 (s, 1.5H), 2.82 (s, 1.5H), 2.63 (s, 1.5H), 2.57 (s, 1.5H). HPLC (max plot) 100%, Rt 2.26 min. UPLC/MS: (MS+) 467.3 ([M+H]+), (MS−) 465.4 ([M−H]−).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403835B2
Source datasetuspto-grants-2016_08
ORD IDord-2d2e57676e634bccb0c9043524e143a6
Source noteuspto-grants-2016_08