Reaction equation
[CH3:1][S:2]([O:5][CH2:6][C:7]([NH:11][CH2:12][C:13]1[CH:14]=C2C(=C3[C:30]=1C=CC=C3)C=CC1C=CC=CC2=1)([CH3:10])[CH2:8][OH:9])(=[O:4])=[O:3].C1[C:48]2[CH:47]=[CH:46][C:45]3[C:36](=[CH:37]C=[C:39]4[C:44]=3[CH:43]=[CH:42][CH:41]=[CH:40]4)[C:35]=2[CH:34]=CC=1C=O.N[C:52](C)(CO)CO>CCO>[CH3:1][S:2]([O:5][CH2:6][C:7]([NH:11][CH2:12][C:13]1[CH:30]=[CH:34][C:35]2[C:36]3[C:45](=[C:44]4[C:39](=[CH:52][CH:37]=3)[CH:40]=[CH:41][CH:42]=[CH:43]4)[CH:46]=[CH:47][C:48]=2[CH:14]=1)([CH3:10])[CH2:8][OH:9])(=[O:4])=[O:3]Participants
5
Procedure
Using the reductive amination procedure outlined in 1C, chrysene-2-carbaldehyde (20D) and 2-amino-2-methyl-1,3-propanediol (Aldrich) gave 2-((2-chrysenylmethyl)amino)-2-methyl-1,3-propanediol methanesulfonate, mp 225°-227° (dec), (abs. EtOH), (C, H, N, S)
Sources & evidence
- ORD record
- ord-26d51dc902e640c5921dda0a3e3876b5
- Source dataset
- uspto-grants-1988_01
- Patent number
- US04719046
Linked notes
Loading…