반응 #640607

ord-d6234bf21990491bb936e9bb05538d6f

반응 방정식

Cl.O=C(NCC1CC1)c1noc2c1CNCC2
4,5,6,7-tetrahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid cyclopropylmethyl amide hydrochloride
O=C(NCC1CC1)c1noc2c1CNCC2
4,5,6,7-tetrahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid cyclopropylmethyl amide
C=CCCC(=O)Cl
4-pentenoyl chloride
C=CCCC(=O)N1CCc2onc(C(=O)NCC3CC3)c2C1
5-pent-4-enoyl-4,5,6,7-tetrahydro-isoxazolo[4,5-c]pyridine-3-carboxylic acid cyclopropylmethyl amide
수율 84.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08048879B2uspto-grants-2011_11