Ammonia → HCID 23518318, compound
Reaction equation
Br[C:2]1[N:3]([C:14]2[N:15]=[CH:16][N:17]=[C:18]([NH2:21])[C:19]=2[N:20]=1)[C@@H:4]1[O:12][C@H:9]([CH2:10][OH:11])[C@@H:7]([OH:8])[C@@:5]1([CH3:13])[OH:6].[NH3:22]>>[NH2:22][C:2]1[N:3]([C:14]2[N:15]=[CH:16][N:17]=[C:18]([NH2:21])[C:19]=2[N:20]=1)[C@@H:4]1[O:12][C@H:9]([CH2:10][OH:11])[C@@H:7]([OH:8])[C@@:5]1([CH3:13])[OH:6]Participants
3
Procedure
A solution of the compound from Step A (38 mg, 0.11 mmol) in liquid ammonia (10 mL) was heated in a stainless steel autoclave at 105° C. for 1 d, then cooled and evaporated. The residue was purified by HPLC [C-18 Phenomenex Luna (10μ; 250×21.2 mm) RP-column; solvents: (A) water, (13) acetonitrile; Linear gradient: 2-35% B in 76 min.] to yield the title compound (12 mg) as a white fluffy material after freeze-drying.
Workup
- temperaturecooled
- customevaporated
- customThe residue was purified by HPLC [C-18 Phenomenex Luna (10μ; 250×21.2 mm) RP-column; solvents: (A) water, (13) acetonitrile; Linear gradient: 2-35% B in 76 min.]
Sources & evidence
- ORD record
- ord-88d416a5724a4e2987ba3d9599684ca7
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07105499B2
Reaction notes
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