3-Amino-1,2-propanediol → HCID 178479730, compound
Reaction equation
[Cl:1][C:2]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=[C:4]([C:5]([NH:7][C:8]2[NH:12][N:11]=[N:10][N:9]=2)=[O:6])[CH:3]=1.[NH2:20][CH2:21][CH:22]([OH:25])[CH2:23][OH:24]>>[ClH:1].[OH:25][CH:22]([CH2:23][OH:24])[CH2:21][NH:20][C:2]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:13]=[C:4]([C:5]([NH:7][C:8]2[NH:12][N:11]=[N:10][N:9]=2)=[O:6])[CH:3]=1Participants
3
Procedure
4(2,3-Dihydroxypropylamino)-N(1H-tetrazol-5-yl)quinaldamide, hydrochloride, m.p. 264° (d) was prepared from 4-chloro-N(1H-tetrazol-5-yl)quinaldamide (Example 2 ) and 3-amino-1,2-propanediol.
Sources & evidence
- ORD record
- ord-1df4806382314a7b86c860951008d94c
- Source dataset
- uspto-grants-1976_01
- Patent number
- US03932416
Reaction notes
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