HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Pentenoyl chloride → HCID 11950281, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Pentenoyl chloride | HCID 4228493 | — |
| Reactant | HCID 57618624 | HCID 57618624 | — |
| Reactant | HCID 67461967 | HCID 67461967 | — |
| Product | HCID 11950281 | HCID 11950281 | 84% |
Reaction Steps
The corresponding base was released from 4,5,6,7-tetrahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid cyclopropylmethyl amide hydrochloride. In a manner similar to general method 3, 170 mg (0.42 mmol) of 4,5,6,7-tetrahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid cyclopropylmethyl amide were reacted with 89 μL (0.89 mmol) of 4-pentenoyl chloride to yield 150 mg (84% of theoretical) of 5-pent-4-enoyl-4,5,6,7-tetrahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid cyclopropylmethyl amide (66), which were obtained in the form of a brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08048879B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-d6234bf21990491bb936e9bb05538d6f |
| Source note | uspto-grants-2011_11 |