3-Hydroxy-3-phenyl-1-butyne → HCID 10184463, compound

HRID 351741

Reaction equation

HRID 351741 reaction equation
[C:1]1([C:7](O)([C:9]#[CH:10])C)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.BrC1[CH:14]=[N+:15]([O-:23])[CH:16]=[C:17]([C:19]([OH:22])([CH3:21])[CH3:20])[CH:18]=1.[CH:24]([NH:27][C:28]([C:30]1[C:39](=[O:40])[C:38]2[C:33](=[N:34][CH:35]=[CH:36][CH:37]=2)[N:32](C2C=CC=C(Br)C=2)[CH:31]=1)=[O:29])([CH3:26])[CH3:25]>>[CH:24]([NH:27][C:28]([C:30]1[C:39](=[O:40])[C:38]2[C:33](=[N:34][CH:35]=[CH:36][CH:37]=2)[N:32]([C:5]2[CH:4]=[CH:3][CH:2]=[C:1]([C:7]#[C:9][C:10]3[CH:14]=[N+:15]([O-:23])[CH:16]=[C:17]([C:19]([OH:22])([CH3:21])[CH3:20])[CH:18]=3)[CH:6]=2)[CH:31]=1)=[O:29])([CH3:25])[CH3:26]

Participants

4

Procedure

Following the procedure of EXAMPLE 15, but substituting N-isopropyl-1-(3-ethynylphenyl)-1,4-dihydro[1,8]naphthyridin-4-one-3-carboxamide from EXAMPLE 5 for 2-phenyl-3-butyn-2-ol, and 3-bromo-5-(1-hydroxy-1-methylethyl)pyridine-N-oxide from Step 2 for N-isopropyl-1-(3-bromophenyl)-1,4-dihydro[1,8]naphthyridin-4-one-3-carboxamide, the N-isopropyl-1-{3-[5-(1-hydroxy-1-methylethyl)-1-oxido-3-pyridinylethynyl]phenyl}-1,4-dihydro[1,8]naphthyridin-4-one-3-carboxamide compound was obtained as a solid.

Sources & evidence

ORD record
ord-2c30c522d0dd4b3c8d46a5d294d2e2e3
Source dataset
uspto-grants-2004_06
Patent number
US06743802B2

Linked notes

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