Methyl 3-(5-formylfuran-2-yl)thiophene-2-carboxylate → HCID 22049384, compound

HRID 2087399Notes

Reaction equation

HRID 2087399 reaction equation
[CH:1]([C:3]1[O:7][C:6]([C:8]2[CH:12]=[CH:11][S:10][C:9]=2[C:13]([O:15][CH3:16])=[O:14])=[CH:5][CH:4]=1)=O.[CH3:17][CH:18]([CH3:34])[C:19]([NH:21][C:22]1[CH:27]=[CH:26][CH:25]=[C:24]([CH:28]2[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]2)[CH:23]=1)=[O:20]>>[C:19]([NH:21][C:22]1[CH:23]=[C:24]([CH:28]2[CH2:29][CH2:30][N:31]([CH2:1][C:3]3[O:7][C:6]([C:8]4[CH:12]=[CH:11][S:10][C:9]=4[C:13]([O:15][CH3:16])=[O:14])=[CH:5][CH:4]=3)[CH2:32][CH2:33]2)[CH:25]=[CH:26][CH:27]=1)(=[O:20])[CH:18]([CH3:34])[CH3:17]

Participants

3

Reactant 2

HCID 2797068Methyl 3-(5-formylfuran-2-yl)thiophene-2-carboxylateHCID 167572552-methyl-N-[3-(4-piperidyl)phenyl]propanamide

Product 1

HCID 22049384HCID 22049384, compound

Procedure

Prepared by Procedure F and Scheme R using methyl 3-(5-formyl-2-furyl)-2-thiophenecarboxylate and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 467.1 (M+H)+.

Workup

  1. customPrepared by Procedure F and Scheme R

Sources & evidence

ORD record
ord-6157ace657b7471dbbaabce544ad75a3
Source dataset
uspto-grants-2004_04
Patent number
US06727264B1

Reaction notes

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