5-tert-Butyl-3-(2-chloro-benzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine → HCID 86683307, compound
Reaction equation
C(C1N=C(N2CCOCC2)C2N=NN(CC3C=CC=CC=3Cl)C=2N=1)(C)(C)C.[C:28]([C:32]1[N:33]=[C:34](Cl)[C:35]2[N:40]=[N:39][N:38]([CH2:41][C:42]3[CH:47]=[CH:46][CH:45]=[CH:44][C:43]=3[Cl:48])[C:36]=2[N:37]=1)([CH3:31])([CH3:30])[CH3:29].Cl.[F:51][C:52]1([F:59])[CH2:56][NH:55][C@@H:54]([CH2:57][OH:58])[CH2:53]1>>[C:28]([C:32]1[N:33]=[C:34]([N:55]2[CH2:56][C:52]([F:59])([F:51])[CH2:53][C@@H:54]2[CH2:57][OH:58])[C:35]2[N:40]=[N:39][N:38]([CH2:41][C:42]3[CH:47]=[CH:46][CH:45]=[CH:44][C:43]=3[Cl:48])[C:36]=2[N:37]=1)([CH3:31])([CH3:30])[CH3:29]Participants
4
Reactant 3
Product 1
Procedure
In analogy to the procedure described for the synthesis of 5-tert-butyl-3-(2-chlorobenzyl)-7-morpholin-4-yl-3H-[1,2,3]triazolo[4,5-d]pyrimidine (example 1, step c), the title compound was prepared from 5-tert-butyl-7-chloro-3-(2-chlorobenzyl)-3H-[1,2,3]triazolo[4,5-d]pyrimidine and (R)-(4,4-difluoropyrrolidin-2-yl)methanol hydrochloride and isolated as white solid. MS (m/e): 437.3 (MH+).
Workup
- customisolated as white solid
Sources & evidence
- ORD record
- ord-55ed981b09a94a94b7cc225dd1ddda3c
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08741906B2
Reaction notes
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