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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364151Generated: October 29, 2026

Cyclohexanone → HCID 16048831, compound

https://huagongshe.com/reaction/1364151

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 66930837HCID 66930837—
CatalystAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 16048831HCID 16048831—

Reaction Steps

To a solution of 1-[4-(5,6,7,8-tetrahydropyrazolo[3,4-d]azepin-2(4H)-yl)phenyl]-2-pyrrolidinone (may be prepared as described in Description 22) (45 mg, 0.15 mmol) in dichloromethane (3 ml) was added cyclohexanone (29 mg, 0.30 mmol) and acetic acid (2 drops). The resulting mixture was stirred at room temperature, under argon, for 20 minutes. Sodium triacetoxyborohydride (64 mg, 0.30 mmol) was added and stirring continued for 22 hours. A further 2 eq. of cyclohexanone (29 mg, 0.30 mmol) was added, and after a further 20 minutes a further 2 eq. of sodium triacetoxyborohydride (64 mg, 0.30 mmol) was added and stirring continued for 3 hours. The resulting crude mixture was diluted with methanol and then purified by SCX, eluting with methanol and then with 2M ammonia/methanol. The basic fractions were combined and solvent evaporated in vacuo to afford the title compound (E22). MS (ES+) m/e 379 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888347B2
Source datasetuspto-grants-2011_02
ORD IDord-3a8c2b08f7fb45e18f6ae20c50a11c79
Source noteuspto-grants-2011_02