HCID 178473533, compound → HCID 178512138, compound
Reaction equation
C(OC([NH:6][C:7]([NH:16][CH2:17][CH2:18][CH2:19][C:20]1[N:21]=[CH:22][NH:23][CH:24]=1)=[N:8][CH2:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11]1)=O)C>Cl>[NH:23]1[CH:24]=[C:20]([CH2:19][CH2:18][CH2:17][NH:16][C:7]([NH:8][CH2:9][CH:10]2[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15]2)=[NH:6])[N:21]=[CH:22]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
1.5 mmol of the compound obtained in Example 52 are brought to reflux for 30 min in 15 ml of 1N hydrochloric acid and are then concentrated to dryness. The residual dry form is crystallized from diethyl ether.
Workup
- concentrationare then concentrated to dryness
- customThe residual dry form is crystallized from diethyl ether
Sources & evidence
- ORD record
- ord-00d36bdc766d4234a70a5b145cf50081
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05708171
Reaction notes
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