6-Bromohexanoyl chloride → HCID 21887654, compound

HRID 722914Notes

Reaction equation

HRID 722914 reaction equation
[CH2:1]1[C:11]2=[C:12]3[C:7](=[CH:8][CH:9]=[CH:10]2)[CH2:6][CH2:5][CH2:4][N:3]3[C:2]1=[O:13].[Br:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20](Cl)=[O:21]>>[Br:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][C:20]([C:9]1[CH:8]=[C:7]2[C:12]3=[C:11]([CH2:1][C:2](=[O:13])[N:3]3[CH2:4][CH2:5][CH2:6]2)[CH:10]=1)=[O:21]

Participants

3

Reactant 2

HCID 898486-Bromohexanoyl chlorideHCID 149184935,6-Dihydro-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one

Product 1

HCID 21887654HCID 21887654, compound

Procedure

Using 5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-2(1H)-one and 6-bromohexanoyl chloride according to the same method as that of Reference Example 1, the title compound (5.13 g) was obtained as colorless crystals having a melting point of 86 to 87° C.

Sources & evidence

ORD record
ord-8bc16575623f457b9da8bd1c384e138f
Source dataset
uspto-grants-2006_11
Patent number
US07138533B2

Reaction notes

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