4-Methyl-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-sulfonyl chloride → (R)-4a-Ethoxymethyl-1-(4-fluorophenyl)-6-[[2H-pyrido[3.2-b]-1,4-oxazin-7-yl]sulfonyl]-1,4,7,8-tetrahydro-1,2,6-triazacyclopenta[b]naphthalene

HRID 1907278Notes

Reaction equation

HRID 1907278 reaction equation
C(OC([N:8]1[CH2:17][CH2:16][C:15]2[C@:10]([CH2:28][O:29][CH2:30][CH3:31])([CH2:11][C:12]3[CH:20]=[N:19][N:18]([C:21]4[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=4)[C:13]=3[CH:14]=2)[CH2:9]1)=O)(C)(C)C.C[N:33]1[CH2:38][CH2:37][O:36][C:35]2[CH:39]=[C:40]([S:43](Cl)(=[O:45])=[O:44])[CH:41]=[N:42][C:34]1=2>>[CH2:30]([O:29][CH2:28][C@@:10]12[CH2:9][N:8]([S:43]([C:40]3[CH:41]=[N:42][C:34]4[N:33]=[CH:38][CH2:37][O:36][C:35]=4[CH:39]=3)(=[O:45])=[O:44])[CH2:17][CH2:16][C:15]1=[CH:14][C:13]1[N:18]([C:21]3[CH:26]=[CH:25][C:24]([F:27])=[CH:23][CH:22]=3)[N:19]=[CH:20][C:12]=1[CH2:11]2)[CH3:31]

Participants

3

Procedure

The title compound was prepared by the method of Preparation 1c using (R)-4a-ethoxymethyl-1-(4-fluorophenyl)-1,4,4a,5,7,8-hexahydro-1,2,6-triazacyclopenta[b]naphthalene-6-carboxylic acid tert-butyl ester and 4-methyl-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazine-7-sulfonyl chloride. LCMS (Method C): 540 (M+H)+, Retention time 11.9 minutes.

Sources & evidence

ORD record
ord-56e57f63d6134578a7edc343be91ae3a
Source dataset
uspto-grants-2013_12
Patent number
US08598154B2

Reaction notes

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