1-Hexadecylthio-3-(3-iodopropylsulfonylamino)-2-methoxypropane → HCID 14835057, compound
Reaction equation
Cl[CH2:2][CH2:3][CH2:4][S:5]([NH:8][CH2:9][CH:10]([NH:29][C:30]([NH:32][CH3:33])=[O:31])[CH2:11][S:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28])(=[O:7])=[O:6].C(SCC(OC)CNS(CCC[I:61])(=O)=O)CCCCCCCCCCCCCCC>>[CH2:13]([S:12][CH2:11][CH:10]([NH:29][C:30]([NH:32][CH3:33])=[O:31])[CH2:9][NH:8][S:5]([CH2:4][CH2:3][CH2:2][I:61])(=[O:7])=[O:6])[CH2:14][CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH3:28]Participants
3
Procedure
3-(3-Chloropropylsulfonylamino)-1-hexadecylthio-2-(3-methylureido)propane IIIf2 is allowed to react and worked up by the same procedure as described in (5). m.p. 70°-71° C. The summary of the experimental condition and the physical data of the product are listed in Table 8.
Workup
- customto react
Sources & evidence
- ORD record
- ord-9638d3b2a4954732b19f133f6e5e82d6
- Source dataset
- uspto-grants-1991_09
- Patent number
- US05047540
Reaction notes
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