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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364159Generated: November 1, 2026

Methanol → 4-(6-Cyclobutyl-5,6,7,8-tetrahydropyrazolo[3,4-d]azepin-2(4H)-yl)benzonitrile

https://huagongshe.com/reaction/1364159

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantCyclobutanoneHCID 14496—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactant4-(5,6,7,8-Tetrahydropyrazolo[3,4-d]azepin-2(4H)-yl)benzonitrileHCID 66930882—
CatalystAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Product4-(6-Cyclobutyl-5,6,7,8-tetrahydropyrazolo[3,4-d]azepin-2(4H)-yl)benzonitrileHCID 16048911—

Reaction Steps

4-(5,6,7,8-Tetrahydropyrazolo[3,4-d]azepin-2(4H)-yl)benzonitrile (may be prepared as described in Description 11) (assumed 0.148 mmol) was dissolved in dichloromethane (2 ml) and acetic acid (2 drops). Cyclobutanone (17 μl, 0.22 mmol) and sodium triacetoxyborohydride (47 mg, 0.22 mmol) were added and the mixture stirred at room temperature for 1 hour. Methanol was added and the solution poured onto a 2 g SCX column which was eluted with methanol then 2M ammonia in methanol. The basic fractions were evaporated and the residue purified by flash chromatography eluting with 0-5% 2M ammonia in methanol/dichloromethane to give the title compound (E32).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888347B2
Source datasetuspto-grants-2011_02
ORD IDord-ffbfa2d8004d4afda1c853efcbbfd7bc
Source noteuspto-grants-2011_02