Hydrochloric Acid → HCID 86672542, compound

HRID 541390Notes

Reaction equation

HRID 541390 reaction equation
[Br:1][CH2:2][C:3]([C:5]1[C:6]([CH:28]2[CH2:31][CH2:30][CH2:29]2)=[CH:7][C:8]([CH3:27])=[C:9]([CH:26]=1)[C:10]([N:12]1[CH2:17][CH2:16][CH:15]([C:18]2[CH:25]=[CH:24][C:21]([C:22]#[N:23])=[CH:20][CH:19]=2)[CH2:14][CH2:13]1)=[O:11])=[O:4].Cl.[F:33]C1(C2C=CC(C#N)=CC=2)CCNCC1.Cl>>[Br:1][CH2:2][C:3]([C:5]1[C:6]([CH:28]2[CH2:31][CH2:30][CH2:29]2)=[CH:7][C:8]([CH3:27])=[C:9]([CH:26]=1)[C:10]([N:12]1[CH2:17][CH2:16][C:15]([C:18]2[CH:19]=[CH:20][C:21]([C:22]#[N:23])=[CH:24][CH:25]=2)([F:33])[CH2:14][CH2:13]1)=[O:11])=[O:4]

Participants

4

Reactant 3

HCID 313Hydrochloric AcidHCID 682888554-(4-Fluoropiperidin-4-yl)benzonitrile hydrochlorideHCID 86672541HCID 86672541, compound2×

Product 1

HCID 86672542HCID 86672542, compound

Procedure

The title compound was prepared using standard chemical manipulations and procedures similar to those used for preparation of 4-(1-(5-(2-bromoacetyl)-4-cyclobutyl-2-methylbenzoyl)piperidin-4-yl)benzonitrile (compound 235.2) but using compound 11.2 HCl salt instead of compound 1.5.

Sources & evidence

ORD record
ord-991b652add274456887b07c372d4e977
Source dataset
uspto-grants-2014_10
Patent number
US08871790B2

Reaction notes

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