Isovaleryl chloride → HCID 23323481, compound

HRID 1381127Notes

Reaction equation

HRID 1381127 reaction equation
[NH2:1][C:2]1[CH:11]=[CH:10][C:9]2[N:8]([CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:7](=[O:19])[N:6]3[CH2:20][CH2:21][N:22]=[C:5]3[C:4]=2[CH:3]=1.[C:23](Cl)(=[O:28])[CH2:24][CH:25]([CH3:27])[CH3:26]>>[C:23]([NH:1][C:2]1[CH:11]=[CH:10][C:9]2[N:8]([CH2:12][C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:7](=[O:19])[N:6]3[CH2:20][CH2:21][N:22]=[C:5]3[C:4]=2[CH:3]=1)(=[O:28])[CH2:24][CH:25]([CH3:27])[CH3:26]

Participants

3

Reactant 2

HCID 66054Isovaleryl chlorideHCID 13035742HCID 13035742, compound

Product 1

HCID 23323481HCID 23323481, compound

Procedure

Preparation analogously to Example 37 from 9-amino-5-oxo-6-benzyl-2,3,5,6-tetrahydroimidazo-[1,2-c]-quinazoline and isovaleric acid chloride.

Sources & evidence

ORD record
ord-dad50221e1d44cd08cef5f9f7a91b1ae
Source dataset
uspto-grants-1986_04
Patent number
US04585772

Reaction notes

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