Methanesulfonyl chloride → HCID 49870573, compound

HRID 333902Notes

Reaction equation

[NH2:1][C:2]([CH3:32])([CH3:31])[C:3]#[C:4][C:5]1[CH:10]=[CH:9][C:8]([C@@H:11]([N:13]2[CH2:18][CH2:17][C@:16]([CH2:25][C:26]([OH:29])([CH3:28])[CH3:27])([C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)[O:15][C:14]2=[O:30])[CH3:12])=[CH:7][CH:6]=1.[CH3:33][S:34](Cl)(=[O:36])=[O:35]>>[OH:29][C:26]([CH3:27])([CH3:28])[CH2:25][C@@:16]1([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[O:15][C:14](=[O:30])[N:13]([C@H:11]([C:8]2[CH:9]=[CH:10][C:5]([C:4]#[C:3][C:2]([NH:1][S:34]([CH3:33])(=[O:36])=[O:35])([CH3:31])[CH3:32])=[CH:6][CH:7]=2)[CH3:12])[CH2:18][CH2:17]1

Participants

Reactant 2

HCID 31297Methanesulfonyl chloride

HCID 49870322HCID 49870322, compound

Product 1

HCID 49870573HCID 49870573, compound

Procedure

The title compound was prepared following a procedure analogous to that described in Example 15 using (S)-3-((S)-1-(4-(3-amino-3-methylbut-1-ynyl)phenyl)ethyl)-6-(2-hydroxy-2-methylpropyl)-6-phenyl-1,3-oxazinan-2-one and methanesulfonyl chloride. LC-MS Method 1 tR=1.53 min, m/z=513, 455; 1H NMR (CDCl3) 1.13 (s, 3H), 1.18 (s, 3H), 1.49 (d, 3H), 1.69 (s, 6H), 2.10-2.45 (5H), 2.83 (m, 1H), 3.14 (s, 3H), 5.66 (q, 1H), 6.92 (d, 2H), 7.17 (d, 2H), 7.30-7.40 (5H)

Sources & evidence

ORD record: ord-e7f5a1019e7744948b813c598a015c21
Source dataset: uspto-grants-2014_11
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08883778B2

Reaction notes

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