3-Amino-1,2-propanediol → HCID 18433013, compound
Reaction equation
[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[C:4]([C:12]2[CH:13]=[C:14]3[C:18](=[CH:19][CH:20]=2)[CH2:17][CH2:16][CH2:15]3)[CH:3]=1.[NH2:21][CH2:22][CH:23]([OH:26])[CH2:24][OH:25]>>[ClH:1].[CH2:17]1[C:18]2[C:14](=[CH:13][C:12]([C:4]3[CH:3]=[C:2]([NH:21][CH2:22][CH:23]([OH:26])[CH2:24][OH:25])[C:11]4[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=4)[N:5]=3)=[CH:20][CH:19]=2)[CH2:15][CH2:16]1Participants
3
Procedure
The title compound, m.p. 157-160° C., MS: m/e=334 (M+), was prepared from 4-chloro-2-indan-5-yl-quinoline and (RS)-3-amino-1,2-propandiol.
Sources & evidence
- ORD record
- ord-6d4ef847dca94a938513b5ddc84caace
- Source dataset
- uspto-grants-2002_08
- Patent number
- US06440995B1
Reaction notes
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