Acrylic Acid → HCID 86655463, compound
Reaction equation
Cl.[CH3:2][O:3][C:4]1[CH:16]=[CH:15][C:7]([CH2:8][C@@H:9]([C:11]([O:13][CH3:14])=[O:12])[NH2:10])=[CH:6][CH:5]=1.[C:17](O)(=[O:20])[CH:18]=[CH2:19].C1CCC(N=C=NC2CCCCC2)CC1.C(N(CC)CC)C>C(Cl)(Cl)Cl>[C:17]([NH:10][C@H:9]([C:11]([O:13][CH3:14])=[O:12])[CH2:8][C:7]1[CH:6]=[CH:5][C:4]([O:3][CH3:2])=[CH:16][CH:15]=1)(=[O:20])[CH:18]=[CH2:19]Participants
6
Procedure
The same procedures as in Example 1 were carried out from the compound obtained in Example 33 (3.3 g), acrylic acid (1.1 mL), DCC (3.4 g), triethylamine (9.5 mL, 68.2 mmol), and chloroform (140 mL), to give the captioned compound (2.1 g, 58%) as crystals.
Sources & evidence
- ORD record
- ord-1f855bd5f4df4e9ab1b2290a6160ee70
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09150510B2
Reaction notes
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