HCID 178419530, compound → HCID 178435269, compound

HRID 1391219Notes

Reaction equation

HRID 1391219 reaction equation
C(NC(=N)SC)(C)C.Br.[CH2:10]([CH:12]1[C:17]2[N:18]=[CH:19][NH:20][C:16]=2[CH2:15][CH2:14][N:13]1[C:21](=[NH:26])[NH:22][CH:23]([CH3:25])[CH3:24])[CH3:11]>>[CH2:10]([CH:12]1[C:17]2[N:18]=[CH:19][NH:20][C:16]=2[CH2:15][CH2:14][N:13]1[C:21](=[NH:26])[NH:22][CH:23]([CH3:25])[CH3:24])[CH3:11]

Participants

3

Reactant 2

HCID 178419530HCID 178419530, compoundHCID 178504036HCID 178504036, compound

Product 1

HCID 178435269HCID 178435269, compound

Procedure

Operating as in Example 22, but employing N-isopropyl-S-methyl-isothiourea, 1.6 g of 4-ethyl-5-(N-isopropyl-guanyl)-4,5,6,7-tetrahydro-imidazo-[4,5-c]-pyridine monohydrobromide (m.p. 280° (dec.)) are obtained.

Workup

  1. customare obtained

Sources & evidence

ORD record
ord-ea5164ec30144b51847970d64e318d94
Source dataset
uspto-grants-1979_02
Patent number
US04141899

Reaction notes

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