Hydrochloric Acid → HCID 15233815, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([O:28][CH3:29])=[C:6]([N:8]2[CH2:13][CH2:12][N:11]([CH2:14][CH:15]([OH:27])[CH2:16][NH:17][C:18]3[N:23]=[C:22]([C:24]([NH2:26])=[O:25])[CH:21]=[CH:20][N:19]=3)[CH2:10][CH2:9]2)[CH:7]=1.Cl>CO>[NH2:26][C:24]([C:22]1[CH:21]=[CH:20][N:19]=[C:18]([NH:17][CH2:16][CH2:15][NH:26][C:24]([C:22]2[CH:21]=[CH:20][N:19]=[C:18]([NH:17][CH2:16][CH:15]([OH:27])[CH2:14][N:11]3[CH2:10][CH2:9][N:8]([C:6]4[CH:7]=[C:2]([Cl:1])[CH:3]=[CH:4][C:5]=4[O:28][CH3:29])[CH2:13][CH2:12]3)[N:23]=2)=[O:25])[N:23]=1)=[O:25]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4.7 g. (11.16 mmol) of (±)-2-[[3-[4-(5-chloro-2-methoxyphenyl) piperazin-1-yl]-2-hydroxypropyl]amino]pyrimidine-4-carboxamide and 450 ml of methanol are introduced into a 1 l round-bottomed flask, a stream of gaseous hydrochloric acid is passed through for a few minutes and the mixture is heated at the reflux temperature of the methanol for 2 h.
Workup
- customis passed through for a few minutes
Sources & evidence
- ORD record
- ord-7a549fd1fcc640f2a177e6e03cadf65c
- Source dataset
- uspto-grants-1994_07
- Patent number
- US05330985
Reaction notes
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