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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214415Generated: November 2, 2026

HCID 23514989, compound → HCID 20644298, compound

https://huagongshe.com/reaction/2214415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23514989HCID 23514989—
ReactantHCID 178440437HCID 178440437—
ReactantHCID 178506544HCID 178506544—
ProductHCID 20644298HCID 20644298—

Reaction Steps

9-{(2R,3R,4R,5R)-3,4-bis(1,1,2,2-tetramethyl-1silapropoxy)-5-[(1,1,2,2-tetramethyl-1-silapropoxy)methyl]oxolan-2-yl}-2-[1-(1-methylethyl)pyrazol-4yl]purine-6-ylamine (16) Compound 16 was prepared in the manner of compound 11 substituting 4-iodo-(1-methylethyl)pyrazole for 4-iodo-benzylpyrazole to afford compound 16: 1H NMR(CDCl3) 0.00 (s, 3H, CH3), 0.01 (s, 3H, CH3), 0.04 (s, 3H, CH3), 0.07 (s, 3H, CH3), 0.11 (s, 3H, CH3), 0.14 (s, 3 H, CH3), 0.78 (s, 9H, t-bu), 0.83 (s, 9H, t-bu), 0.91 (s, 9H, t-bu), 1.55(d, 6H, C(CH3)2), 3.8 (d, 1H), 4.05 (d, 1H), 4.08–4.15(m, 1H), 4.30–4.32 (m, 1H), 4.44–4.56 (m, 2H), 5.55(bs, 1H, D2O exchangeable), 6.05 (s, 1H), 8.05 (s, 1H), 8.10 (s, 1H), 8.2 (s, 1H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109180B2
Source datasetuspto-grants-2006_09
ORD IDord-b4be843922354999a17072579c6ea692
Source noteuspto-grants-2006_09