Piperazine → HCID 178487976, compound

HRID 258667Notes

Reaction equation

HRID 258667 reaction equation
Cl.[N:2]1([C:8]2[C:25]3[C:20](=[CH:21][CH:22]=[CH:23][CH:24]=3)[N:19]=[C:10]([C:11]([NH:13][C:14]3[NH:18][N:17]=[N:16][N:15]=3)=[O:12])[CH:9]=2)[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.N1CCNC[CH2:27]1.[Cl:32]C1C2C(=CC=CC=2)N=C([C:36](NC2NN=NN=2)=[O:37])C=1>>[ClH:32].[CH3:36][O:37][C:23]1[CH:24]=[C:25]2[C:20](=[CH:21][CH:22]=1)[N:19]=[C:10]([C:11]([NH:13][C:14]1[NH:18][N:17]=[N:16][N:15]=1)=[O:12])[CH:9]=[C:8]2[N:2]1[CH2:3][CH2:4][N:5]([CH3:27])[CH2:6][CH2:7]1

Participants

4

Reactant 3

HCID 4837PiperazineHCID 178479728HCID 178479728, compoundHCID 178522680HCID 178522680, compound

Product 1

HCID 178487976HCID 178487976, compound

Procedure

4-Piperazino-N(1H-tetrazol-5-yl)quinaldamide hydrochloride, m.p. 320° (d), was prepared in a similar way from piperazine and 4-chloro-N(1H-tetrazol-5-yl)quinaldamide.

Sources & evidence

ORD record
ord-38c9967f84364923a86fa817ca1494ef
Source dataset
uspto-grants-1977_07
Patent number
US04034075

Reaction notes

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