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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Oxo-azetidine-1-carboxylic acid tert-butyl ester | HCID 1519404 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | HCID 86727313 | HCID 86727313 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86727314 | HCID 86727314 | 44% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09115151B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-a53cb706ada543fdb2c0e129379013e1 |
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| Source note | uspto-grants-2015_08 |
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