HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2060786Generated: October 31, 2026
HCID 57504918, compound → HCID 66848225, compound
https://huagongshe.com/reaction/2060786
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 57504918 | HCID 57504918 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66848225 | HCID 66848225 | — |
Reaction Steps
To a solution of racemic N-((4aRS,6RS,7aSR)-6-(tert-butyldimethylsilyloxy)-7a-(3′-methoxybiphenyl-3-yl)-4,4a,5,6,7,7a-hexahydrocyclopenta[d][1,3]thiazin-2-yl)benzamide (1.47 g, 2.31 mmol) in acetonitrile (6 mL) is added 20-25% aqueous fluorosilicic acid (2.82 g, 4.62 mmol) and the resulting mixture is stirred at room temperature for 3 h. The reaction is diluted with ethyl acetate and quenched with saturated aqueous sodium bicarbonate. The mixture is washed with water and brine. The organic layer is dried over sodium sulfate, filtered, and concentrated under reduced pressure. The crude product is purified by silica gel chromatography eluting with a linear gradient of 10% to 60% ethyl acetate in hexanes over 40 minutes to give the title compound as a racemic mixture (0.709 g, 64%). ES/MS m/e: 459 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278441B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-11a8877ebbe64bbcb1ac47a486019d05 |
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| Source note | uspto-grants-2012_10 |
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