Cyclopropanecarboxylic acid → HCID 178521734, compound
Reaction equation
[CH:1]1([NH:8][C:9]2[O:10][CH2:11][C:12]3[CH:18]=[C:17]([NH2:19])[CH:16]=[CH:15][C:13]=3[N:14]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH:20]1([C:23](O)=[O:24])[CH2:22][CH2:21]1>>[CH:1]1([NH:8][C:9]2[O:10][CH2:11][C:12]3[CH:18]=[C:17]([NH:19][C:23]([CH:20]4[CH2:22][CH2:21]4)=[O:24])[CH:16]=[CH:15][C:13]=3[N:14]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1Participants
3
Procedure
Prepared from N2-cycloheptyl-4H-benzo[d][1,3]oxazine-2,6-diamine (example 92) (200 mg, 0.77 mmol) and cyclopropanecarboxylic acid (80 mg, 0.93 mmol) according to the procedure described for example 93. Obtained the title compound as an off-white foam (104 mg, 41%), MS (ISP) m/e=328.4 [(M+H)+].
Sources & evidence
- ORD record
- ord-c585b15944804a3eab503a8a6c47d681
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163740B2
Reaction notes
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