HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 519044Generated: October 30, 2026
HCID 86727349, compound → HCID 90220745, compound
https://huagongshe.com/reaction/519044
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 86727349 | HCID 86727349 | — |
| Reactant | HCID 86727353 | HCID 86727353 | — |
| Product | HCID 86727411 | HCID 86727411 | 47% |
| Product | HCID 90220745 | HCID 90220745 | 50% |
Reaction Steps
Racemic 3-(7-isopropyl-4-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yloxy)-azetidine-1-carboxylic acid tert-butyl ester (prepared from the corresponding bromide (Example #65, Step G) with similar procedure as descried in Example #57, Step A-B, 0.090 g, 0.210 mmol) was separated by chiral SFC (Table 2, Method 7) to give 3-(7-isopropyl-4(S)-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yloxy)-azetidine-1-carboxylic acid tert-butyl ester (Enantiomer 1, SFC (Table 1, Method 13) Rt=1.572 min.; 0.045 g, 50%) and 3-(7-isopropyl-4(R)-methyl-3-oxo-2,3,4,10-tetrahydro-9-oxa-1,2,4a-triaza-phenanthren-6-yloxy)-azetidine-1-carboxylic acid tert-butyl ester (Enantiomer 2, SFC (Table 1, Method 13) Rt=2.104 min, 0.042 g, 47%).
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-2d99be04262b4817aeb3cd0047950506 |
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| Source note | uspto-grants-2015_08 |
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