HCID 18357553, compound → HCID 18357678, compound

Reaction equation

[O:1]1[C:9]2[CH:8]=[CH:7][N:6]=[CH:5][C:4]=2[C:3]([C:10]2[CH:17]=[CH:16][CH:15]=[CH:14][C:11]=2[CH:12]=[O:13])=[N:2]1.ClC1C=CN=CC=1CC1C=CC=CC=1C(OCC)OCC>>[O:1]1[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[C:3]([C:10]2[CH:17]=[CH:16][CH:15]=[CH:14][C:11]=2[CH:12]=[O:13])=[N:2]1

Participants

Reactant 2

HCID 18357553HCID 18357553, compound

HCID 18357679HCID 18357679, compound

Product 1

HCID 18357678HCID 18357678, compound

Procedure

2-(Isoxazolo[4,5-c]pyridin-3-yl)-benzaldehyde starting from (4-chloropyridin-3-yl)-2-(diethoxymethyl)-phenylmethane; 1H-NMR (200 MHz, CDCl3) d 10.26 (CHO).

Sources & evidence

ORD record: ord-62760510846343e8bf49e90b59d2dc2e
Source dataset: uspto-grants-2000_06
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06080773

Reaction notes

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