Pyrrolidine → HCID 19428542, compound

HRID 1078962Notes

Reaction equation

HRID 1078962 reaction equation
Cl[C:2]1[CH:7]=[C:6]([Cl:8])[N:5]=[C:4]([N:9]2[C:14]([CH3:16])([CH3:15])[CH2:13][CH2:12][CH2:11][C:10]2([CH3:18])[CH3:17])[N:3]=1.[NH:19]1[CH2:23][CH2:22][CH2:21][CH2:20]1>>[Cl:8][C:6]1[CH:7]=[C:2]([N:19]2[CH2:23][CH2:22][CH2:21][CH2:20]2)[N:3]=[C:4]([N:9]2[C:14]([CH3:16])([CH3:15])[CH2:13][CH2:12][CH2:11][C:10]2([CH3:18])[CH3:17])[N:5]=1

Participants

3

Reactant 2

HCID 31268PyrrolidineHCID 19428508HCID 19428508, compound

Product 1

HCID 19428542HCID 19428542, compoundYield 75.08%

Procedure

4,6-Dichloro-2-(2,2,6,6-tetramethyl-1-piperidinyl)pyrimidine is reacted with pyrrolidine as described in Example 12 to give the title compound in a yield of 75.08%, m.p.: 130°-135° C.

Sources & evidence

ORD record
ord-738924c7a5e94f249cdf865ac8c9a351
Source dataset
uspto-grants-1996_08
Patent number
US05550240

Reaction notes

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