Cyclopropanemethanamine → HCID 18753267, compound
Reaction equation
Cl[C:2]1[C:7]([C:8]#[N:9])=[C:6]([Cl:10])[N:5]=[C:4]([NH:11][CH2:12][CH2:13][OH:14])[N:3]=1.[NH2:15][CH2:16][CH:17]1[CH2:19][CH2:18]1.C(N(C(C)C)C(C)C)C>O1CCOCC1>[Cl:10][C:6]1[C:7]([C:8]#[N:9])=[C:2]([NH:15][CH2:16][CH:17]2[CH2:19][CH2:18]2)[N:3]=[C:4]([NH:11][CH2:12][CH2:13][OH:14])[N:5]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
In analogy to the procedure described in example 38b, 4,6-dichloro-2-(2-hydroxy-ethylamino)-pyrimidine-5-carbonitrile was treated with aminomethyl-cyclopropane in dioxane in the presence of N-ethyl-diisopropylamine at 90° C. to yield 4-chloro-6-(cyclo-propylmethyl-amino)-2-(2-hydroxy-ethylamino)-pyrimidine-5-carbonitrile as an amorphous, white solid; MS: [M+H]+=268.
Sources & evidence
- ORD record
- ord-f67e23b077de44a7869218fb93627bb8
- Source dataset
- uspto-grants-2004_01
- Patent number
- US06673795B2
Reaction notes
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