Methylamine → HCID 68964529, compound

HRID 2116358Notes

Reaction equation

HRID 2116358 reaction equation
CC1C=CC(S(O[CH2:12][CH:13]2[CH2:17][C:16]3[CH:18]=[C:19]([CH3:29])[CH:20]=[C:21]([C:22]4[CH:27]=[CH:26][C:25]([F:28])=[CH:24][CH:23]=4)[C:15]=3[O:14]2)(=O)=O)=CC=1.[CH3:30][NH2:31]>>[F:28][C:25]1[CH:26]=[CH:27][C:22]([C:21]2[C:15]3[O:14][CH:13]([CH2:12][NH:31][CH3:30])[CH2:17][C:16]=3[CH:18]=[C:19]([CH3:29])[CH:20]=2)=[CH:23][CH:24]=1

Participants

3

Reactant 2

HCID 6329MethylamineHCID 86599323HCID 86599323, compound

Product 1

HCID 68964529HCID 68964529, compound

Procedure

The title compound was prepared (0.028 g, 25%) following the general procedure of Example 390 as a white solid, hydrochloride salt from (±)-[7-(4-fluorophenyl) 5-methyl-2,3-dihydro-1-benzofuran-2-yl]methyl 4-methylbenzenesulfonate (0.15 g, 0.36 mmol) and methylamine (0.112 g, 3.6 mmol). mp 206-208° C.

Sources & evidence

ORD record
ord-f0d4db081e3b49cb912ea502c235f4b2
Source dataset
uspto-grants-2008_10
Patent number
US07435837B2

Reaction notes

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