Diisopropylethylamine → [6-Cyclopropylmethoxy-5-(3,3-difluoro-azetidin-1-yl)-pyridin-2-yl]-(4-hydroxy-4-methyl-piperidin-1-yl)-methanone

HRID 624923Notes

Reaction equation

HRID 624923 reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[N:11]=[C:10]([C:12]([OH:14])=O)[CH:9]=[CH:8][C:7]=2[N:15]2[CH2:18][C:17]([F:20])([F:19])[CH2:16]2)[CH2:3][CH2:2]1.Cl.[CH3:22][C:23]1([OH:29])[CH2:28][CH2:27][NH:26][CH2:25][CH2:24]1.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.[B-](F)(F)(F)F.CCN(C(C)C)C(C)C>>[CH:1]1([CH2:4][O:5][C:6]2[N:11]=[C:10]([C:12]([N:26]3[CH2:27][CH2:28][C:23]([OH:29])([CH3:22])[CH2:24][CH2:25]3)=[O:14])[CH:9]=[CH:8][C:7]=2[N:15]2[CH2:18][C:17]([F:20])([F:19])[CH2:16]2)[CH2:2][CH2:3]1

Participants

5

Procedure

In analogy to the procedure described in Example 47 b), 6-cyclopropylmethoxy-5-(3,3-difluoro-azetidin-1-yl)-pyridine-2-carboxylic acid (Example 1 b)) was reacted with 4-methylpiperidin-4-ol hydrochloride (586375-35-1) in the presence of TBTU and DIEA to obtain the title compound as colorless oil; MS (EI): m/e=382.6 [MH+].

Sources & evidence

ORD record
ord-b10aa73213ec4c98a85bf95735be1cd1
Source dataset
uspto-grants-2016_04
Patent number
US09303012B2

Reaction notes

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