SA07280303B1 - مشتقات بها استبدال من (3as, 7as)-1-3A,4,5,6,7-Hexahydro-3H-Benzoimidazol-2-One والعمليات الخاصة بتحضيرها، والتركيبات المحتوية عليها والتطبيقات - Google Patents

Info

Publication number

SA07280303B1

SA07280303B1 SA7280303A SA07280303A SA07280303B1 SA 07280303 B1 SA07280303 B1 SA 07280303B1 SA 7280303 A SA7280303 A SA 7280303A SA 07280303 A SA07280303 A SA 07280303A SA 07280303 B1 SA07280303 B1 SA 07280303B1

Authority

SA

Saudi Arabia

Prior art keywords

piperidyl

hexahydro

compound

benzoimidazol

benzimidazol

Prior art date

2006-06-09

Links

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• Global Dossier
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• RWIIUBCMPVZLBA-UHFFFAOYSA-N 1,3,3a,4,5,6,7,7a-octahydrobenzimidazol-2-one Chemical compound C1CCCC2NC(=O)NC21 RWIIUBCMPVZLBA-UHFFFAOYSA-N 0.000 claims description 54
• 125000000753 cycloalkyl group Chemical group 0.000 claims description 49
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 40
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 39
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 34
• 125000005936 piperidyl group Chemical group 0.000 claims description 29
• YFEOSTXFQCDCAR-UHFFFAOYSA-N 3-(1,2,3,6-tetrahydropyridin-4-yl)-1h-benzimidazol-2-one Chemical compound O=C1NC2=CC=CC=C2N1C1=CCNCC1 YFEOSTXFQCDCAR-UHFFFAOYSA-N 0.000 claims description 27
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 27
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• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 15
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• SXVOJMDLKZHJBL-ROUUACIJSA-N ethyl 4-[4-[(3as,7as)-2-oxo-3a,4,5,6,7,7a-hexahydro-3h-benzimidazol-1-yl]piperidin-1-yl]piperidine-1-carboxylate Chemical compound C1CN(C(=O)OCC)CCC1N1CCC(N2C(N[C@H]3CCCC[C@@H]32)=O)CC1 SXVOJMDLKZHJBL-ROUUACIJSA-N 0.000 claims 1
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