HCID 12400041, compound → HCID 54407166, compound

HRID 543637Notes

Reaction equation

HRID 543637 reaction equation
C1([C:7]2[C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][C:12]=3[NH:11][C:10]3[N:18]=[CH:19][CH:20]=[CH:21][C:9]=3[N:8]=2)C=CC=CC=1.[CH3:22][O:23][C:24](=[O:31])[N:25]([CH2:27][CH2:28][CH2:29]Cl)[CH3:26]>>[CH3:22][O:23][C:24](=[O:31])[N:25]([CH3:26])[CH2:27][CH2:28][CH2:29][N:11]1[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=2[CH:7]=[N:8][C:9]2[CH:21]=[CH:20][CH:19]=[N:18][C:10]1=2

Participants

3

Reactant 2

HCID 12400041HCID 12400041, compoundHCID 135626384HCID 135626384, compound

Product 1

HCID 54407166HCID 54407166, compound

Procedure

The title compound is prepared by reacting 6-phenyl-11H-pyrido[2,3-b][1,4]benzodiazepine and (3-chloropropyl)methylcarbamic acid methyl ester.

Sources & evidence

ORD record
ord-c515fd4d307c41518583b0f92f53ef75
Source dataset
uspto-grants-1984_05
Patent number
US04447361

Reaction notes

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