3-Chlorophenoxazine → 3-Chloro-10-[1-(1-pyrrolin-2-YL)-2-pyrrolin-2-YL]phenoxazine hydrochloride

HRID 1764226Notes

Reaction equation

HRID 1764226 reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:6][C:7]3[C:12]([O:13][C:14]=2[CH:15]=1)=[CH:11][CH:10]=[CH:9][CH:8]=3.Cl.Cl[C:18]1[N:19]([C:23]2[CH2:27][CH2:26][CH2:25][N:24]=2)[CH2:20][CH2:21][CH:22]=1>>[ClH:1].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([C:18]3[N:19]([C:23]4[CH2:27][CH2:26][CH2:25][N:24]=4)[CH2:20][CH2:21][CH:22]=3)[C:7]3[C:12]([O:13][C:14]=2[CH:15]=1)=[CH:11][CH:10]=[CH:9][CH:8]=3

Participants

3

Reactant 2

HCID 189139213-ChlorophenoxazineHCID 203071382-Chloro-1-(1-pyrrolin-2-yl) 2-pyrroline hydrochloride

Product 1

HCID 203071793-Chloro-10-[1-(1-pyrrolin-2-YL)-2-pyrrolin-2-YL]phenoxazine hydrochloride

Procedure

Reaction of 3-chlorophenoxazine with 2-chloro-(1-pyrrolin-2-yl)pyrroline hydrochloride according to the procedure of Example 7 affords 3-CHLORO-10-[1-(1-PYRROLIN-2-YL)-2-PYRROLIN-2-YL]PHENOXAZINE HYDROCHLORIDE, m.p. 262.5°-270° C. (dec.)(corr.), from ethanol-ether.

Sources & evidence

ORD record
ord-d797b551c81142bf9726cf868a39653f
Source dataset
uspto-grants-1978_09
Patent number
US04115571

Reaction notes

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