HCID 11067172, compound → HCID 19601624, compound

HRID 398952Notes

Reaction equation

HRID 398952 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]2[C:8]([CH:11]3[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][C:19]4[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=4)[CH2:13][CH2:12]3)=[CH:9][NH:10][C:5]2=[CH:4][CH:3]=1.Cl.[N:26]1[CH:31]=[CH:30][C:29]([C:32](Cl)=[O:33])=[CH:28][CH:27]=1>>[N:26]1[CH:31]=[CH:30][C:29]([C:32]([NH:1][C:2]2[N:7]=[C:6]3[C:8]([CH:11]4[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][C:19]5[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=5)[CH2:13][CH2:12]4)=[CH:9][NH:10][C:5]3=[CH:4][CH:3]=2)=[O:33])=[CH:28][CH:27]=1

Participants

3

Reactant 2

HCID 11067172HCID 11067172, compoundHCID 12262826Isonicotinoyl chloride hydrochloride

Product 1

HCID 19601624HCID 19601624, compound

Procedure

Beginning with 0.015 gm (0.047 mMol) 5-amino-3-(1-(2-phenyleth-1-yl)piperidin-4-yl)pyrrolo[3,2-b]pyridine and 0.011 mL (0.061 mMol) 4-pyridinecarbonyl chloride hydrochloride, the title compound was prepared essentially by the procedure described in Example 7.

Sources & evidence

ORD record
ord-f0083631aa744a66b03a53b85d7bab51
Source dataset
uspto-grants-1998_10
Patent number
US05817671

Reaction notes

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