2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amine → HCID 44200771, compound
Reaction equation
[Cl:1][C:2]1[CH:29]=[CH:28][C:5]([C:6]([NH:8][NH:9][C:10](=O)[C@H:11]([NH:16][C:17]2[CH:22]=[CH:21][C:20]([C:23]#[N:24])=[C:19]([Cl:25])[C:18]=2[CH3:26])[C:12]([OH:15])([CH3:14])[CH3:13])=[O:7])=[CH:4][CH:3]=1.CCN(P1(N(C)CCCN1C)=NC(C)(C)C)CC>C1COCC1>[Cl:25][C:19]1[C:18]([CH3:26])=[C:17]([NH:16][C@@H:11]([C:10]2[O:7][C:6]([C:5]3[CH:28]=[CH:29][C:2]([Cl:1])=[CH:3][CH:4]=3)=[N:8][N:9]=2)[C:12]([OH:15])([CH3:14])[CH3:13])[CH:22]=[CH:21][C:20]=1[C:23]#[N:24]Participants
Procedure
The crude material of (R)-4-chloro-N′-(2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxy-3-methylbutanoyl)benzohydrazide (intermediate 15a) (230 mg, 0.53 mmol) was added to THF (50 mL) stirred at room temperature. PS-BEMP (721 mg, 1.59 mmol base) was added to the solution followed by slow addition of p-TSCl (111 mg, 0.58 mmol). The reaction mixture was stirred for 1 h and the progress of the reaction was monitored by TLC. After the completion of the reaction the BEMP reagent was filtered off and the solution concentrated to get the crude material. The crude material was chromatographed with hexanes:EtOAc (6:4) to provide the product (740 mg):1H NMR(500 MHz, CDCl3, δ in ppm) 7.95 (d, J=9 Hz, 2H), 7.50 (d, J=9 Hz, 2H), 7.39 (d, J=9 Hz, 1H), 6.63 (d, J=9 Hz, 1H), 5.37 (d, J=9 Hz, 1H), 4.74 (d, J=9 Hz, 1H), 2.36 (s, 3H), 1.52 (s, 3H), 1.36 (s, 3H).
Workup
- additionfollowed by slow addition of p-TSCl (111 mg, 0.58 mmol)
- stirringThe reaction mixture was stirred for 1 h
- filtrationwas filtered off
- concentrationthe solution concentrated
- customto get the crude material
- customThe crude material was chromatographed with hexanes:EtOAc (6:4)
Sources & evidence
- ORD record
- ord-652ae86affe442f296e742f643e76dee
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08268872B2
Reaction notes
Loading…