HCID 12439914, compound → HCID 20436444, compound

HRID 1153766Notes

Reaction equation

HRID 1153766 reaction equation
[CH2:1]([N:3]1[CH2:9][CH2:8][C:7](O[Si](C)(C)C)=[C:6](O[Si](C)(C)C)[CH2:5][CH2:4]1)[CH3:2].[ClH:20].Cl.[C:22]([CH:25]([NH2:31])[C:26]([O:28][CH2:29][CH3:30])=[O:27])(=[NH:24])[NH2:23]>>[ClH:20].[ClH:20].[NH2:24][C:22]1[C:25]([C:26]([O:28][CH2:29][CH3:30])=[O:27])=[N:31][C:7]2[CH2:8][CH2:9][N:3]([CH2:1][CH3:2])[CH2:4][CH2:5][C:6]=2[N:23]=1

Participants

3

Reactant 2

HCID 12439914HCID 12439914, compoundHCID 13037030HCID 13037030, compound

Product 1

HCID 20436444HCID 20436444, compound

Procedure

This compound was prepared analogous to Example 22 from 1-ethyl-2,3,6,7-tetrahydro-4,5-bis(trimethylsilyloxy)azepine and ethyl 2-amidino-2-aminoacetate dihydrochloride.

Sources & evidence

ORD record
ord-afa66f4386a64d5aaf3e59b6b7c075dd
Source dataset
uspto-grants-1984_12
Patent number
US04486433

Reaction notes

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