HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2382701Generated: October 31, 2026
Tert-butyl acetoacetate → HCID 86643503, compound
https://huagongshe.com/reaction/2382701
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl acetoacetate | HCID 15538 | — |
| Reactant | 2-Chloro-5-(2,3,4,5-tetrahydro-benzo[b]azepine-1-sulfonyl)-phenylamine | HCID 23120301 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86643503 | HCID 86643503 | 79.2% |
Reaction Steps
To 2-chloro-5-(2,3,4,5-tetrahydro-benzo[b]azepine-1-sulfonyl)-phenylamine (1.0 g, 3 mmol, step 4B) in dry toluene (60 mL) was added tert-butyl acetoacetate (0.75 mL, 4.5 mmol) and 4-dimethyl-aminopyridine (0.37 g, 3 mmol). The mixture was refluxed under N2 for 16 hrs. After the removal of toluene, the reaction residue was repartitioned with ethyl acetate (100 mL) and water (50 mL). The organic layer was washed with sat. NH4Cl (2×50 mL) and brine (2×50 mL) and was dried over MgSO4. Concentration and purification by silica gel column chromatography eluting with hexane/ethyl acetate (3/1 to 1/1) yielded N-[2-chloro-5-(2,3,4,5-tetrahydro-benzo[b]azepine-1-sulfonyl)-phenyl]-3-oxo-butyramide as yellowish solid (1.0 g). MS: 421.0 (M+H)+; tR=2.74 min (method 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08263588B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-38883c3583994db89d5b72ac82df5e8f |
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| Source note | uspto-grants-2012_09 |
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