Hydrochloric Acid → HCID 68075551, compound
Reaction equation
C([O:3][C:4](=[O:33])[CH2:5][N:6]1[CH:10]=[C:9]([C:11]2[O:15][N:14]=[C:13]([C:16]3([C:20]4[CH:25]=[CH:24][C:23]([C:26]5[CH:27]=[N:28][C:29]([NH2:32])=[N:30][CH:31]=5)=[CH:22][CH:21]=4)[CH2:19][CH2:18][CH2:17]3)[N:12]=2)[CH:8]=[N:7]1)C.C1COCC1.O.[OH-].[Li+].Cl>O.CO>[NH2:32][C:29]1[N:30]=[CH:31][C:26]([C:23]2[CH:24]=[CH:25][C:20]([C:16]3([C:13]4[N:12]=[C:11]([C:9]5[CH:8]=[N:7][N:6]([CH2:5][C:4]([OH:33])=[O:3])[CH:10]=5)[O:15][N:14]=4)[CH2:19][CH2:18][CH2:17]3)=[CH:21][CH:22]=2)=[CH:27][N:28]=1Participants
7
Conditions
- Temperature
- 40 °C
Procedure
R102 (784 mg, 1.76 mmol) is treated with THF (7.0 mL), methanol (1.5 mL), water (3.0 mL), and lithium hydroxide monohydrate (222 mg, 5.28 mmol) and the resulting mixture is stirred at 40° C. for 1.5 hours. The mixture is then treated with 1N hydrochloric acid (5.28 mL, 5.28 mmol) and concentrated in vacuo to afford R103 (960 mg).
Workup
- concentrationconcentrated in vacuo
- customto afford R103 (960 mg)
Sources & evidence
- ORD record
- ord-4ab3f196e74d496f925f97d549d60eda
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580829B2
Reaction notes
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