2-Pyrrolidin-1-ylmethyl-piperidine → 5,10-Dihydro-5-[[2-[(1-pyrrolidinyl)methyl]-1-piperidinyl]-acetyl]-11H-dibenzo[b,e][1,4]diazepin-11-one

HRID 465062Notes

Reaction equation

HRID 465062 reaction equation
Cl[CH2:2][C:3]([N:5]1[C:11]2[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=2[C:9](=[O:16])[NH:8][C:7]2[CH:17]=[CH:18][CH:19]=[CH:20][C:6]1=2)=[O:4].[N:21]1([CH2:26][CH:27]2[CH2:32][CH2:31][CH2:30][CH2:29][NH:28]2)[CH2:25][CH2:24][CH2:23][CH2:22]1>C(O)(C)C>[N:21]1([CH2:26][CH:27]2[CH2:32][CH2:31][CH2:30][CH2:29][N:28]2[CH2:2][C:3]([N:5]2[C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=3[C:9](=[O:16])[NH:8][C:7]3[CH:17]=[CH:18][CH:19]=[CH:20][C:6]2=3)=[O:4])[CH2:25][CH2:24][CH2:23][CH2:22]1

Participants

4

Reactant 2

HCID 27605412-Pyrrolidin-1-ylmethyl-piperidineHCID 100854195-(chloroacetyl)-5,10-dihydro-11H-dibenzo[b,e][1,4]diazepin-11-one

Product 1

HCID 135785605,10-Dihydro-5-[[2-[(1-pyrrolidinyl)methyl]-1-piperidinyl]-acetyl]-11H-dibenzo[b,e][1,4]diazepin-11-one

Reagents, catalysts & solvents 1

HCID 3776IsopropanolSolvent

Procedure

The title compound is prepared analogously to Example 2 from 5-(chloroacetyl)-5,10-dihydro-11H-dibenzo[b,e][1,4]diazepin-11-one and 2-[(1-pyrrolidinyl)methyl]piperidine to give colorless crystals, mp. 199°-201° C. (isopropanol/activated charcoal).

Sources & evidence

ORD record
ord-711934a3e9b749f5b2dcdd02faf2cc66
Source dataset
uspto-grants-1985_10
Patent number
US04550107

Reaction notes

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