(Iodomethyl)cyclopropane → HCID 117622753, compound

HRID 56702Notes

Reaction equation

HRID 56702 reaction equation
[Cl:1][C:2]1[C:3]([C:17]2[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:18]=2[C:24]#[N:25])=[CH:4][C:5](=[O:16])[N:6]([CH2:8][C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH:7]=1.I[CH2:27][CH:28]1[CH2:30][CH2:29]1>>[Cl:1][C:2]1[C:3]([C:17]2[CH:22]=[C:21]([Cl:23])[CH:20]=[CH:19][C:18]=2[C:24]#[N:25])=[CH:4][C:5](=[O:16])[N:6]([CH:8]([CH2:27][CH:28]2[CH2:30][CH2:29]2)[C:9]([O:11][C:12]([CH3:15])([CH3:14])[CH3:13])=[O:10])[CH:7]=1

Participants

3

Reactant 2

HCID 2763048(Iodomethyl)cyclopropaneHCID 117622894tert-Butyl [5-chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]acetate

Product 1

HCID 117622753HCID 117622753, compound

Procedure

349 mg (0.91 mmol) of tert-butyl [5-chloro-4-(5-chloro-2-cyanophenyl)-2-oxopyridin-1(2H)-yl]acetate and 216 mg (1.18 mmol) of (iodomethyl)cyclopropane were reacted according to General Method 7A. Yield: 245 mg (62% of theory)

Sources & evidence

ORD record
ord-d7afdfdcdc424800a64cd2bf490b4e49
Source dataset
uspto-grants-2016_09
Patent number
US09434690B2

Reaction notes

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