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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 421608Generated: November 1, 2026

Cyclopentylamine → HCID 57639337, compound

https://huagongshe.com/reaction/421608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentylamineHCID 2906—
ReactantDiisopropylamineHCID 7912—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 57639250HCID 57639250—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57639337HCID 5763933766%

Reaction Steps

1-Hydroxy-4-{2-[(methylethyl)amino]-8-[(2,4,6-trifluorophenyl)amino]purin-9-yl}cyclohexanecarboxylic acid (0.200 g, 0.4 mmol) was dissolved in 4 mL of dry THF. Cyclopentyl amine (0.079 mL, 0.8 mmol) was added neat followed by di-isopropyl amine (0.105 mL, 0.6 mmol). Benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (BOP) was added last, as a solid in one portion at room temperature (0.177 g, 0.4 mmol). The reaction was complete within 10 min as confirmed by LC-MS. DMF was removed under reduced pressure. The residue was triturated in saturated aqueous sodium bicarbonate. The resulting beige solid was collected by filtration and washed with water. The crude product was re-crystallized from hot methanol-water. The crystals were dried in vacuum oven. (141 mg, 66% yield) M+1: 532.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101588B2
Source datasetuspto-grants-2012_01
ORD IDord-0c167197bfb942c08b13197f199d748a
Source noteuspto-grants-2012_01