Reaction #1199728

ord-9ac54b14f8f54d179e137a75cdd9db02

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

Following the procedure described in Example 9, part B above but using equivalent amounts of 5-chloro-4,6,7-trifluoro-1,3-diiminoisoindoline and 2-(2-methylpiperidino)-4-imino-2-thiazoline hydrochloride in place of 1,3-diiminoisoindoline and 2-piperidino-4-imino-2-thiazoline hydrochloride respectively, there is obtained as the product 1-imino-5-chloro-4,6,7-trifluoro-3-[2-(2-methylpiperidino)-4-imino-2-thiazolin-5-ylidene]isoindoline hydrochloride.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04122261uspto-grants-1978_10