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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714017Generated: October 31, 2026

Acetic Acid → methyl 14-cyclohexyl-7-(4-methylpiperazin-1-yl)-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate

https://huagongshe.com/reaction/1714017

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium HydroxideHCID 14798—
Reactant1-MethylpiperazineHCID 53167—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactantmethyl 14-cyclohexyl-7-oxo-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylateHCID 50994368—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Productmethyl 14-cyclohexyl-7-(4-methylpiperazin-1-yl)-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylateHCID 68505443—

Reaction Steps

To a solution of methyl 14-cyclohexyl-7-oxo-7,8-dihydro-6H-indolo[1,2-e][1,5]benzoxazocine-11-carboxylate (prepared as described in Example 9, Step 4) in DCM (0.04 M), were added 3.0 eq of 1-methylpiperazine and 4.5 eq acetic acid, followed by 1.5 eq. of solid sodium triacetoxyborohydride. NaOH (20 eq, 1 N) was added after 2 h, and after stirring for 5 min the mixture was taken into EtOAc and washed with water and brine. Drying over sodium sulfate and concentration in vacuo gave the crude product, which was used without any further purification; MS (ES+) m/z 488 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795247B2
Source datasetuspto-grants-2010_09
ORD IDord-66e980d4d6c742458ec2e12af811344e
Source noteuspto-grants-2010_09