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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1513096Generated: November 4, 2026

HCID 68515720, compound → HCID 59309806, compound

https://huagongshe.com/reaction/1513096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68515720HCID 68515720—
ReactantHCID 86641291HCID 86641291—
CatalystHCID 178503042HCID 178503042—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59309806HCID 59309806—
ProductHCID 68515720HCID 68515720—
ProductHCID 86641291HCID 86641291—

Reaction Steps

9-[2-Chloro-5-(2-fluoro-6-methoxybenzyloxy)-4-methoxyphenyl]-2-chloromethyl-6-methoxy-7,9-dihydro-8H-purin-8-one was prepared in a similar manner to that described in Example 410 using the corresponding starting materials. 2-Azidomethyl-9-[2-chloro-5-(2-fluoro-6-methoxybenzyloxy)-4-methoxyphenyl]-6-methoxy-7,9-dihydro-8H-purin-8-one was prepared in a similar manner to that described in Example 413 using 9-[2-chloro-5-(2-fluoro-6-methoxybenzyloxy)-4-methoxyphenyl]-2-chloromethyl-6-methoxy-7,9-dihydro-8H-purin-8-one instead of 9-[2-chloro-5-(2,3-difluoro-6-methoxybenzyloxy)-4-methoxyphenyl]-2-chloromethyl-6-methoxy-7,9-dihydro-8H-purin-8-one. To 2-azidomethyl-9-[2-chloro-5-(2-fluoro-6-methoxybenzyloxy)-4-methoxyphenyl]-6-methoxy-7,9-dihydro-8H-purin-8-one (0.1 g) were added tetrahydrofuran (10 mL) and 10% platinum-carbon powder (50 mg), and the mixture was stirred at room temperature under a hydrogen atmosphere for 4 hours. The insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure to give the title compound (94 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217069B2
Source datasetuspto-grants-2012_07
ORD IDord-92e4fba2a8be403f82de2f1b0c8e5267
Source noteuspto-grants-2012_07