Morpholine → HCID 58466120, compound

HRID 336012Notes

Reaction equation

HRID 336012 reaction equation
Br[C:2]1[CH:3]=[C:4]2[C@@:15]3([CH2:19][O:18][C:17]([NH2:20])=[N:16]3)[C:14]3[CH:13]=[C:12](Cl)[N:11]=[C:10]([F:22])[C:9]=3[O:8][C:5]2=[CH:6][CH:7]=1.[F:23][C:24]1[C:29](B(O)O)=[CH:28][CH:27]=[CH:26][N:25]=1.[NH:33]1[CH2:38][CH2:37][O:36][CH2:35][CH2:34]1>>[F:22][C:10]1[C:9]2[O:8][C:5]3[C:4]([C@@:15]4([CH2:19][O:18][C:17]([NH2:20])=[N:16]4)[C:14]=2[CH:13]=[C:12]([N:33]2[CH2:38][CH2:37][O:36][CH2:35][CH2:34]2)[N:11]=1)=[CH:3][C:2]([C:29]1[C:24]([F:23])=[N:25][CH:26]=[CH:27][CH:28]=1)=[CH:7][CH:6]=3

Participants

4

Reactant 3

HCID 8083MorpholineHCID 27832702-Fluoropyridine-3-boronic acidHCID 58466258(S)-7-bromo-3-chloro-1-fluoro-5'H-spiro[chromeno[2,3-c]pyridine-5,4' oxazol]-2'-amine

Product 1

HCID 58466120HCID 58466120, compound

Procedure

The titled compound was synthesized by steps analogous to those described in Method CC4 above using (S)-7-bromo-3-chloro-1-fluoro-5′H-spiro[chromeno[2,3-c]pyridine-5,4′ oxazol]-2′-amine (prepared as described in Method BB33), 2-fluoropyridin-3-ylboronic acid, and morpholine.

Sources & evidence

ORD record
ord-029c58773d874dfdb2bd4027edc8fb98
Source dataset
uspto-grants-2014_11
Patent number
US08883782B2

Reaction notes

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