Imidazole → HCID 25215199, compound

HRID 2194783Notes

Reaction equation

ClC1C=C(C#N)C2C=[CH:7][N:8]([C:11]3[N:12]([CH2:22][CH3:23])[C:13](=[O:21])[NH:14][C:15](=[O:20])[C:16]=3[CH:17]([CH3:19])[CH3:18])[C:9]=2[CH:10]=1.[NH:26]1C=CN=C1>>[CH2:22]([N:12]1[C:11]([N:8]2[CH:9]=[CH:10][N:26]=[CH:7]2)=[C:16]([CH:17]([CH3:18])[CH3:19])[C:15](=[O:20])[NH:14][C:13]1=[O:21])[CH3:23]

Participants

Reactant 2

HCID 795Imidazole

HCID 67050527HCID 67050527, compound

Product 1

HCID 25215199HCID 25215199, compound

Procedure

This compound was made by a procedure similar to that used to prepare 6-chloro-1-(3-ethyl-5-isopropyl-2,6-dioxo-1,2,3,6-tetrahydro-pyrimidin-4-yl)-1H-indole-4-carbonitrile (90), except that imidazole was used instead of 6-chloro-1H-indole-4-carbonitrile. LC-MS shows 249.1 (M+1). 1H NMR (300 MHz, CDCl3): δ 9.03 (br, 1H), 7.60 (m, 1H), 7.32 (m, 1H), 7.00 (m, 1H), 3.40 (m, 2H), 2.08 (m, 1H), 1.19 (m, 9H).

Sources & evidence

ORD record: ord-ebfc6e8fa67643019e89e5203524903f
Source dataset: uspto-grants-2012_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08334295B2

Reaction notes

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