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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 915942Generated: October 31, 2026

Benzyl methyl(piperidin-4-yl)carbamate hydrochloride → Benzyl 1-[4-(3-cyclohexyl-1-methyl-4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-6-yl)-3-ethoxyphenyl]-4-piperidinyl(methyl)carbamate

https://huagongshe.com/reaction/915942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl methyl(piperidin-4-yl)carbamate hydrochlorideHCID 18677745—
ReactantHCID 136005963HCID 136005963—
ProductBenzyl 1-[4-(3-cyclohexyl-1-methyl-4-oxo-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-6-yl)-3-ethoxyphenyl]-4-piperidinyl(methyl)carbamateHCID 13633321077%

Reaction Steps

The same reaction procedure as in Example 27 was performed, except that the compound obtained in Example 85 was used in place of the compound obtained in Example 26, and benzyl methyl(4-piperidinyl)carbamate hydrochloride was used in place of N-methylpiperazine. In this manner, 234 mg (77%) of the captioned compound was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07268128B2
Source datasetuspto-grants-2007_09
ORD IDord-0bfbadf1fe8b467f8152c5da47e8a2a7
Source noteuspto-grants-2007_09