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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363973Generated: October 29, 2026

2-Iodoadenosine → 2-{3-[1-(Phenoxycarbonyl)piperidin-4-yl]propyn-1-yl}adenosine

https://huagongshe.com/reaction/1363973

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodoadenosineHCID 169662—
ReactantPhenyl 4-(prop-2-ynyl)piperidine-1-carboxylateHCID 57838938—
Product2-{3-[1-(Phenoxycarbonyl)piperidin-4-yl]propyn-1-yl}adenosineHCID 25093963—

Reaction Steps

Batch: AB-9-97. Phenyl 4-(prop-2-ynyl)piperidine-1-carboxylate, batch JR28-11 (0.329 g, 1.352 mmol) was added to a solution of 2-iodoadenosine (0.513 g, 1.305 mmol) according to general procedure 2. Yield: 54.5 mg, 82%. 1H NMR (CD3OD) δ 8.30 (s, 1H), 7.38-7.06 (3×m, 5H), 5.94 (d, 1H), 4.71 (m, 1H), 4.32-4.17 (2×m, 7H), 3.92-3.72 (2×d, 2H), 3.10-2.90 (2×bt, 4H), 2.48 (d, 5H), 1.93 (2×m, 5H). m/z MH+=509.18. HPLC rt=5.3 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888329B2
Source datasetuspto-grants-2011_02
ORD IDord-e79b0238521b41758b1e65caa0ba214c
Source noteuspto-grants-2011_02