Hydrochloric Acid → HCID 66594242, compound
Reaction equation
C(OC(=O)[NH:7][C:8]1([CH2:16][CH2:17][C:18]2[CH:23]=[CH:22][C:21](CCCC3CCCCC3)=[C:20]([C:33]([F:36])([F:35])[F:34])[CH:19]=2)[CH2:13][O:12]C(C)(C)[O:10][CH2:9]1)(C)(C)C.[ClH:38].[CH2:39]([OH:41])[CH3:40]>>[ClH:38].[NH2:7][C:8]([CH2:16][CH2:17][C:18]1[CH:23]=[CH:22][C:21]([O:41][CH2:39][CH2:40][CH2:17][CH:18]2[CH2:23][CH2:22][CH2:21][CH2:20][CH2:19]2)=[C:20]([C:33]([F:34])([F:35])[F:36])[CH:19]=1)([CH2:9][OH:10])[CH2:13][OH:12]Participants
4
Conditions
- Temperature
- 80 °C
Procedure
Compound 9-2 (760 mg) was dissolved in ethanol (15 ml), concentrated hydrochloric acid (3 ml) was added, and the mixture was stirred at 80° C. for 2.5 hr. The reaction mixture was concentrated, and the residue was washed with diethyl ether to give the object product (525 mg) as a white powder. MS(ESI)m/z: 404[M+H]
Workup
- concentrationThe reaction mixture was concentrated
- washthe residue was washed with diethyl ether
Sources & evidence
- ORD record
- ord-262d53da32904aff97934f14b046e652
- Source dataset
- uspto-grants-2012_03
- Patent number
- US08129361B2
Reaction notes
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