4-Aminofuro[3,2-c]pyridine-2-carbonitrile → 4-Amino-2-(aminomethyl)furo[3,2-c]pyridine

HRID 2304304Notes

Reaction equation

HRID 2304304 reaction equation
[NH2:1][C:2]1[C:7]2[CH:8]=[C:9]([C:11]#[N:12])[O:10][C:6]=2[CH:5]=[CH:4][N:3]=1.NC1C2C(=CC=C(CN)C=2)C=CN=1>>[NH2:1][C:2]1[C:7]2[CH:8]=[C:9]([CH2:11][NH2:12])[O:10][C:6]=2[CH:5]=[CH:4][N:3]=1

Participants

3

Reactant 2

HCID 226658084-Aminofuro[3,2-c]pyridine-2-carbonitrileHCID 226658411-Amino-7-isoquinolinemethanamine

Product 1

HCID 226657294-Amino-2-(aminomethyl)furo[3,2-c]pyridine

Procedure

This compound was prepared from 4-amino-furo[3,2-c]pyridine-2-carbonitrile (5.7 g), using the procedure described for 1-amino-7-(aminomethyl)isoquinoline. Yield: 3.5 g (60%); yellow crystals; m.p. 142-144° C., EI-MS: 163 (M+).

Sources & evidence

ORD record
ord-a42921bc8980429996ca87710af6507b
Source dataset
uspto-grants-2002_08
Patent number
US06432955B1

Reaction notes

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