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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518968Generated: October 30, 2026

3-Oxo-azetidine-1-carboxylic acid tert-butyl ester → HCID 86727314, compound

https://huagongshe.com/reaction/518968

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 86727313HCID 86727313—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 86727314HCID 8672731444%

Reaction Steps

A solution of 6-amino-4,7-dimethyl-2,10-dihydro-9-oxa-1,2,4a-triaza-phenanthren-3-one ((Example #54, Step E, 0.060 g, 0.24 mmol) and 3-oxo-azetidine-1-carboxylic acid tert-butyl ester (0.083 g, 0.41 mmol) in MeOH (4.5 mL) and acetic acid (0.5 mL) was stirred at ambient temperature for 1 h. Sodium cyanoborohydride (0.031 g, 0.41 mmol) was added and the resulting dark solution was stirred at ambient temperature for 14 h. The solvent was removed in vacuo to give the crude product, which was purified by preparative TLC (eluting with 33% EtOAc in petroleum ether) to give 3-(4,7-dimethyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-ylamino)-azetidine-1-carboxylic acid tert-butyl ester (0.042 g, 44%) as an off-white solid. LC/MS (Table 1, Method 2) Rt=1.065 min.; MS m/z: 424 [M+23]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115151B2
Source datasetuspto-grants-2015_08
ORD IDord-a53cb706ada543fdb2c0e129379013e1
Source noteuspto-grants-2015_08