N-methyl-1-pyridin-2-ylpropan-2-amine → HCID 21520968, compound

HRID 918389Notes

Reaction equation

HRID 918389 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][N:7]=[C:6]2Cl.[CH3:16][NH:17][CH:18]([CH3:26])[CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=1>>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][N:7]=[C:6]2[N:17]([CH:18]([CH3:26])[CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][N:21]=1)[CH3:16]

Participants

3

Reactant 2

HCID 203877N-methyl-1-pyridin-2-ylpropan-2-amineHCID 27693644-Chloro-6,7-dimethoxyquinazoline

Product 1

HCID 21520968HCID 21520968, compound

Procedure

Reaction of 6,7-dimethoxy-4-chloroquinazoline with 2-(2-[N-methylamino]prop-1-yl)pyridine, according to the procedure of Example I, yielded the title compound, isolated as its dihydrochloride dihydrate, m.p. 242°-5°C.

Sources & evidence

ORD record
ord-f7a4fe77989d400f88428893ba08ca77
Source dataset
uspto-grants-1976_07
Patent number
US03971783

Reaction notes

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