HCID 19420759, compound → HCID 19420735, compound

HRID 1734693Notes

Reaction equation

HRID 1734693 reaction equation
Cl.[O:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[N:4]=[C:3]1[C:11]1[CH:16]=[CH:15][C:14]([CH2:17][CH2:18]N)=[CH:13][CH:12]=1.O1C2C=CC=CC=2[N:22]=[C:21]1[C:29]1C=CC(CCCC#N)=CC=1.O1C2C=CC=CC=2N=C1C1C=CC(CCCCN)=CC=1>>[O:2]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[N:4]=[C:3]1[C:11]1[CH:12]=[CH:13][C:14]([CH:17]([CH3:18])[CH2:29][CH2:21][NH2:22])=[CH:15][CH:16]=1

Participants

4

Reactant 3

HCID 19420759HCID 19420759, compoundHCID 19420763HCID 19420763, compoundHCID 19420775HCID 19420775, compound

Product 1

HCID 19420735HCID 19420735, compound

Procedure

When 4-(benzoxazol-2-yl)benzyl cyanide of Example 42, Step D is replaced by 4-[4-(benzoxazol-2-yl)phenyl]butyronitrile, then the product prepared is 4-[4-(benzoxazol-2-yl)phenyl]butylamine (m.p. 220° C. dec.).

Workup

  1. customthe product prepared

Sources & evidence

ORD record
ord-4214d25e583d467da75797f31a73381b
Source dataset
uspto-grants-1996_07
Patent number
US05534532

Reaction notes

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