HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dichlorobenzaldehyde → HCID 19980858, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dichlorobenzaldehyde | HCID 35745 | — |
| Reactant | 2-(N-Benzyl-N-methylamino)ethyl 3-amino-2-butenoate | HCID 12529188 | — |
| Reactant | tert-Butyl 6-oxo-1,4-thiazepane-4-carboxylate 1,1-dioxide | HCID 19980844 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19980858 | HCID 19980858 | 50.3% |
Reaction Steps
A mixture of 4-N-(t-butyloxycarbonyl)-1,1-dioxo-2,3,4,5,6,7-hexahydro-1,4-thiazepin-6-one (8.39 g, 31.9 mmole) from Example 6, 2,3-dichlorobenzaldehyde (5.58 g, 31.9 mmole) and 2-(N-benzyl-N-methylamino)ethyl 3-aminocrotonate (7.91 31.9 mmole) were heated to reflux in 40 mL of ethanol for 17 hours. The reaction was cooled to room temperature, filtered, and the solid washed with 50 mL of ether to obtain the title compound (10.72 g, 50% yield) D.C.I.M.S. (M+H) 668.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05075440 |
| Source dataset | uspto-grants-1991_12 |
| ORD ID | ord-816ded081e6e484c8454bdc2c8480857 |
| Source note | uspto-grants-1991_12 |