Phenylacetylene → HCID 53245750, compound

Reaction equation

Br[C:2]1[CH:3]=[N:4][C:5]2[N:6]([N:8]=[C:9]([N:11]3[CH2:16][CH2:15][O:14][CH2:13][CH2:12]3)[N:10]=2)[CH:7]=1.[C:17]1([C:23]#[CH:24])[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1>>[N:11]1([C:9]2[N:10]=[C:5]3[N:4]=[CH:3][C:2]([C:24]#[C:23][C:17]4[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=4)=[CH:7][N:6]3[N:8]=2)[CH2:16][CH2:15][O:14][CH2:13][CH2:12]1

Participants

Reactant 2

HCID 10821Phenylacetylene

HCID 58316703HCID 58316703, compound

Product 1

HCID 53245750HCID 53245750, compound

Procedure

The title compound, a light brown solid, MS: m/e=306.1 (M+H+), can be prepared in accordance with the general method of example 1 from 6-bromo-2-morpholin-4-yl-[1,2,4]triazolo[1,5-a]pyrimidine (example 47, step 1) and phenylacetylene.

Sources & evidence

ORD record: ord-e0549218818d4f438ee8d835480784e3
Source dataset: uspto-grants-2015_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08933094B2

Reaction notes

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