Diethyl cyanophosphonate → HCID 58980937, compound

HRID 1181714Notes

Reaction equation

HRID 1181714 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH2:11][N:12]1[C:20]([C:21]2[N:25]([CH3:26])[CH:24]=[C:23]([C:27]([OH:29])=O)[CH:22]=2)=[C:19]2[C:14]([N:15]([CH2:33][CH:34]([CH3:36])[CH3:35])[C:16](=[O:32])[N:17]([CH3:31])[C:18]2=[O:30])=[N:13]1.[CH3:37][N:38]1[CH2:43][CH2:42][N:41]([CH2:44][CH2:45][CH2:46][NH2:47])[CH2:40][CH2:39]1.C(P(=O)(OCC)OCC)#N>>[Cl:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][CH:6]=[C:5]2[CH2:11][N:12]1[C:20]([C:21]2[N:25]([CH3:26])[CH:24]=[C:23]([C:27]([NH:47][CH2:46][CH2:45][CH2:44][N:41]3[CH2:40][CH2:39][N:38]([CH3:37])[CH2:43][CH2:42]3)=[O:29])[CH:22]=2)=[C:19]2[C:14]([N:15]([CH2:33][CH:34]([CH3:35])[CH3:36])[C:16](=[O:32])[N:17]([CH3:31])[C:18]2=[O:30])=[N:13]1

Participants

4

Reactant 3

HCID 76257Diethyl cyanophosphonateHCID 783281-(3-Aminopropyl)-4-methylpiperazineHCID 589810635-{2-[(5-chloro-1H-indol-3-yl)methyl]-7-isobutyl-5-methyl-4,6-dioxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-d]pyrimidin-3-yl}-1-methyl-1H-pyrrole-3-carboxylic acid

Product 1

HCID 58980937HCID 58980937, compound

Procedure

This compound was synthesized by the reaction of 5-{2-[(5-chloro-1H-indol-3-yl)methyl]-7-isobutyl-5-methyl-4,6-dioxo-4,5,6,7-tetrahydro-2H-pyrazolo[3,4-d]pyrimidin-3-yl}-1-methyl -1H-pyrrole-3-carboxylic acid and 3-(4-methylpiperazin-1-yl)propylamine using diethyl cyanophosphonate as a coupling reagent Mass: 648.20 (M+H).

Sources & evidence

ORD record
ord-8f263cd0c1484aa190c4f13415800b32
Source dataset
uspto-grants-2007_10
Patent number
US07285558B2

Reaction notes

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