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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214413Generated: October 28, 2026

HCID 23514989, compound → HCID 20644301, compound

https://huagongshe.com/reaction/2214413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23514989HCID 23514989—
ReactantHCID 178462439HCID 178462439—
ReactantHCID 178506544HCID 178506544—
ProductHCID 20644301HCID 20644301—

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-pentylpyrazol-4-yl]purine-6ylamine (14) Compound 14 was prepared in the manner of compound 11 substituting 4-iodo-pentylpyrazole for 4-iodo-benzylpyrazole to afford compound 14:1 H 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, 3H, CH3), 0.78 (s, 9H, t-bu), 0.80 (t, 3H), 0.83 (s, 9H, t-bu), 0.91 (s, 9H, t-bu), 1.25–1.40 (m, 4H), 1.85–1.95 (m, 2H), 3.82 (d, 1H), 4.08 (d, 1H), 4.20–4.28 (m, 3H), 4.32–4.34 (m, 1H), 4.55–4.57 (m, 1H), 5.35 (m, 2H), 5.70 (bs, 2H, D20 exchangeable), 6.08 (d, 1H), 7.28–7.40 (m, 5H), 8.05 (s, 1H), 8.15 (s, 1H), 8.20 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109180B2
Source datasetuspto-grants-2006_09
ORD IDord-1a7302b466b64f4396ce2205a58847eb
Source noteuspto-grants-2006_09