Ethylamine → HCID 52939307, compound
Reaction equation
[NH2:1][C:2]1[N:11]=[C:10]([C:12]([N:14]2[CH2:22][C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH2:15]2)=[O:13])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:23]([CH3:30])([CH2:27][CH2:28][CH3:29])[C:24]([OH:26])=O)[CH:8]=2)[N:3]=1.[CH2:31]([NH2:33])[CH3:32]>>[NH2:1][C:2]1[N:11]=[C:10]([C:12]([N:14]2[CH2:22][C:21]3[C:16](=[CH:17][CH:18]=[CH:19][CH:20]=3)[CH2:15]2)=[O:13])[C:9]2[C:4](=[CH:5][CH:6]=[C:7]([C:23]([CH3:30])([CH2:27][CH2:28][CH3:29])[C:24]([NH:33][CH2:31][CH3:32])=[O:26])[CH:8]=2)[N:3]=1Participants
3
Procedure
(Preparation by reaction of 2-[2-amino-4-(isoindoline-2-carbonyl)quinazolin-6-yl-2-methylpentanoic acid [“A67”] with ethylamine);
Sources & evidence
- ORD record
- ord-86ea71f8c2074c309afe6f37cbb34381
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906930B2
Reaction notes
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