HCID 21161874, compound → HCID 178467877, compound
Reaction equation
O[CH2:2][NH:3][C:4](=[O:11])[C:5]([CH2:7][CH:8]([CH3:10])[CH3:9])=[CH2:6].[P:12]([S-:25])([SH:24])([S:14][CH2:15][CH2:16][CH:17]([O:21][CH2:22][CH3:23])[O:18][CH2:19][CH3:20])=S>>[CH2:22]([O:21][CH:17]([O:18][CH2:19][CH3:20])[CH2:16][CH2:15][S:14][PH:12]([S:25][CH2:2][NH:3][C:4](=[O:11])[CH:5]([CH2:6][S:25][PH:12]([S:14][CH2:15][CH2:16][CH:17]([O:18][CH2:19][CH3:20])[O:21][CH2:22][CH3:23])=[S:24])[CH2:7][CH:8]([CH3:10])[CH3:9])=[S:24])[CH3:23]Participants
3
Procedure
Following the procedure of Example 1, 0.4 mole of N-hydroxymethyl-2-isobutylacrylamide is reacted with 0.8 mole of diethoxypropyl hydrogen phosphorotetrathioate to yield N-(diethoxypropylthiophosphinothioylthiomethyl) 2-(diethoxypropylthiophosphinothioylthiomethyl)-4-methylvaleramide.
Sources & evidence
- ORD record
- ord-9c4627db2fd64a418d7bb1614487cb84
- Source dataset
- uspto-grants-1977_06
- Patent number
- US04032461
Reaction notes
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