ethyl 5-(4-chlorophenyl)-2-formyl-3-furoate → HCID 22049407, compound

HRID 2087364Notes

Reaction equation

HRID 2087364 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:12][C:11]([CH:13]=O)=[C:10]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH:9]=2)=[CH:4][CH:3]=1.[CH3:20][CH:21]([CH3:37])[C:22]([NH:24][C:25]1[CH:30]=[CH:29][CH:28]=[C:27]([CH:31]2[CH2:36][CH2:35][NH:34][CH2:33][CH2:32]2)[CH:26]=1)=[O:23]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[O:12][C:11]([CH2:13][N:34]3[CH2:35][CH2:36][CH:31]([C:27]4[CH:28]=[CH:29][CH:30]=[C:25]([NH:24][C:22](=[O:23])[CH:21]([CH3:20])[CH3:37])[CH:26]=4)[CH2:32][CH2:33]3)=[C:10]([C:15]([O:17][CH2:18][CH3:19])=[O:16])[CH:9]=2)=[CH:6][CH:7]=1

Participants

3

Procedure

Prepared by Procedure F and Scheme R using ethyl 5-(4-chlorophenyl)-2-formyl-3-furoate and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 509.0 (M+H)+.

Workup

  1. customPrepared by Procedure F and Scheme R

Sources & evidence

ORD record
ord-a46599de5f504a32af8b6b9fe3c6607c
Source dataset
uspto-grants-2004_04
Patent number
US06727264B1

Reaction notes

Loading…