HCID 19106942, compound → HCID 178440186, compound

HRID 248634Notes

Reaction equation

HRID 248634 reaction equation
[C:1]([C:3]1[NH:7][C:6]([CH2:8][CH2:9][CH3:10])=[N:5][C:4]=1[N:11]1[C:15]([Cl:16])=[CH:14][CH:13]=[C:12]1[Cl:17])#[N:2].C1(C(C2C=CC=CC=2)(C2C=CC=CC=2)C[N:26]2[C:30]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=3[C:37]3[CH:42]=[CH:41][C:40]([CH2:43]Br)=[CH:39][CH:38]=3)=[N:29][N:28]=[N:27]2)C=CC=CC=1>>[C:1]([C:3]1[N:7]([CH2:43][C:40]2[CH:41]=[CH:42][C:37]([C:32]3[CH:33]=[CH:34][CH:35]=[CH:36][C:31]=3[C:30]3[NH:26][N:27]=[N:28][N:29]=3)=[CH:38][CH:39]=2)[C:6]([CH2:8][CH2:9][CH3:10])=[N:5][C:4]=1[N:11]1[C:15]([Cl:16])=[CH:14][CH:13]=[C:12]1[Cl:17])#[N:2]

Participants

3

Reactant 2

HCID 19106942HCID 19106942, compoundHCID 67859265HCID 67859265, compound

Product 1

HCID 178440186HCID 178440186, compound

Procedure

Using the procedure from Example 13, 5-cyano-4-(2,5-dichloro-1H-pyrrol-1-yl)-2-propylimidazole (Example 30) and N-triphenylethyl-5-[4'-(bromomethyl)bipheyl-2-yl]tetrazole (Example 12) are reacted and deprotected to give the title compound.

Workup

  1. customare reacted

Sources & evidence

ORD record
ord-657d8343304d4584af7336703dc49378
Source dataset
uspto-grants-1993_05
Patent number
US05210211

Reaction notes

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