Diethylcarbamoyl chloride → HCID 178464310, compound

HRID 2374560Notes

Reaction equation

[NH2:1][C:2]1[C:3]([C:7]2[NH:26][C:10]3=[CH:11][C:12]4[C:13]([CH2:24][CH3:25])([CH2:22][CH3:23])[C:14](=[O:21])[N:15]([CH:18]([CH3:20])[CH3:19])[C:16]=4[CH:17]=[C:9]3[N:8]=2)=[N:4][NH:5][CH:6]=1.[CH2:27]([N:29]([CH2:33][CH3:34])[C:30](Cl)=[O:31])[CH3:28]>>[CH2:24]([C:13]1([CH2:22][CH3:23])[C:12]2[CH:11]=[C:10]3[NH:26][C:7]([C:3]4[C:2]([NH:1][C:30](=[O:31])[N:29]([CH2:33][CH3:34])[CH2:27][CH3:28])=[CH:6][NH:5][N:4]=4)=[N:8][C:9]3=[CH:17][C:16]=2[N:15]([CH:18]([CH3:20])[CH3:19])[C:14]1=[O:21])[CH3:25]

Participants

Reactant 2

HCID 6916Diethylcarbamoyl chloride

HCID 178436694HCID 178436694, compound

Product 1

HCID 178464310HCID 178464310, compound

Procedure

3-[3-(7,7-Diethyl-5-isopropyl-6-oxo-1,5,6,7-tetrahydro-imidazo[4,5-f]indol-2-yl)-1H-pyrazol-4-yl]-1,1-diethyl-urea was prepared using 2-(4-amino-1H-pyrazol-3-yl)-7,7-diethyl-5-isopropyl-5,7-dihydro-1H-imidazo[4,5-f]indol-6-one (150 mg, 0.43 mmol) and diethylcarbamoyl chloride (58 mg, 0.43 mmol). 12 mg (6%) %) of the title compound were obtained.

Workup

custom3-[3-(7,7-Diethyl-5-isopropyl-6-oxo-1,5,6,7-tetrahydro-imidazo[4,5-f]indol-2-yl)-1H-pyrazol-4-yl]-1,1-diethyl-urea was prepared

Sources & evidence

ORD record: ord-5b588eb87ae94837b534b4dd811906fb
Source dataset: uspto-grants-2008_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07462639B2

Reaction notes

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