Ethylamine → HCID 52939305, 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]2C(=C[CH:6]=[C:7]([CH:23]3[CH2:27][CH2:26][CH2:25][CH:24]3C(O)=O)[CH:8]=2)N=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:31](=[CH:32][CH:6]=[C:7]([C:23]3([C:12]([NH:14][CH2:15][CH3:16])=[O:13])[CH2:27][CH2:26][CH2:25][CH2:24]3)[CH:8]=2)[N:33]=1Participants
3
Procedure
(Preparation by reaction of 2-[2-amino-4-(isoindoline-2-carbonyl)quinazolin-6-yl]cyclopentanecarboxylic acid [“A68”] with ethylamine);
Sources & evidence
- ORD record
- ord-fbe099450ea54d86bf54000415793ffe
- Source dataset
- uspto-grants-2014_12
- Patent number
- US08906930B2
Reaction notes
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