Pyridine → HCID 178488812, compound

HRID 985813Notes

Reaction equation

HRID 985813 reaction equation
C1(O[C:8](=[O:27])[NH:9][C:10]2[S:11][C:12]3[C:18]([CH:19]4[CH2:24][O:23][CH2:22][CH2:21][O:20]4)=[CH:17][CH:16]=[C:15]([O:25][CH3:26])[C:13]=3[N:14]=2)C=CC=CC=1.[CH3:28][NH:29][C@H:30]1[CH2:35][CH2:34][C@H:33]([OH:36])[CH2:32][CH2:31]1.N1C=CC=CC=1>C(Cl)(Cl)Cl>[O:20]1[CH2:21][CH2:22][O:23][CH2:24][CH:19]1[C:18]1[C:12]2[S:11][C:10]([NH:9][C:8](=[O:27])[N:29]([C@H:30]3[CH2:35][CH2:34][C@H:33]([OH:36])[CH2:32][CH2:31]3)[CH3:28])=[N:14][C:13]=2[C:15]([O:25][CH3:26])=[CH:16][CH:17]=1

Participants

5

Reactant 3

HCID 1049PyridineHCID 20769454(+)-(7-[1,4]Dioxan-2-yl-4-methoxy-benzothiazol-2-yl)-carbamic acid phenyl esterHCID 178484843HCID 178484843, compound

Product 1

HCID 178488812HCID 178488812, compound

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent2×

Procedure

From (+)-(7-[1,4]dioxan-2-yl-4-methoxy-benzothiazol-2-yl)-carbamic acid phenyl ester with trans-4-methylamino-cyclohexanol and pyridine in chloroform. [α]D20=+20.5° (c=1.02, CHCl3), ES-MS m/e (%): 422 (M+H+, 100).

Sources & evidence

ORD record
ord-73ab58048bae4d3aa8012e26b495fcf9
Source dataset
uspto-grants-2005_03
Patent number
US06872833B2

Reaction notes

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