HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 388541Generated: October 30, 2026
Aminoacetaldehyde dimethyl acetal → HCID 178495894, compound
https://huagongshe.com/reaction/388541
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aminoacetaldehyde dimethyl acetal | HCID 89728 | — |
| Reactant | HCID 67547565 | HCID 67547565 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178495894 | HCID 178495894 | — |
Reaction Steps
A solution of 4-amino-8-benzyl-1-[4-fluoro-4′-(methylsulfonyl)biphenyl-2-yl]-7-methyl-1,3,8-triazaspiro[4.5]dec-3-en-2-one (50 mg, 0.10 mmol) in 2,2-dimethoxyethylamine (2.0 ml) was sealed and allowed to stir at 85° C. for 18 h. The temperature was increased to 110° C., and the reaction was allowed to stir for an additional 16 h. The reaction was diluted with EtOAc and washed with brine. The organic portion was dried over sodium sulfate, filtered, and concentrated in vacuo to yield 8-benzyl-4-[(2,2-dimethoxyethyl)amino]-1-[4-fluoro-4′-(methylsulfonyl)biphenyl-2-yl]-7-methyl-1,3,8-triazaspiro[4.5]dec-3-en-2-one. LCMS (M+H) 609.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08377954B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-341fa07134824e02b377d02a53ec4546 |
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| Source note | uspto-grants-2013_02 |
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