(3S)-3-methylmorpholine → HCID 58203790, compound

HRID 1190350Notes

Reaction equation

HRID 1190350 reaction equation
[NH:1]1[CH:5]=[C:4]([C:6]2[CH:22]=[CH:21][C:9]3[C:10]4[N:11]=[C:12]([C:18](O)=[O:19])[S:13][C:14]=4[CH2:15][CH2:16][O:17][C:8]=3[CH:7]=2)[CH:3]=[N:2]1.[CH3:23][C@H:24]1[CH2:29][O:28][CH2:27][CH2:26][NH:25]1>>[CH3:23][C@H:24]1[CH2:29][O:28][CH2:27][CH2:26][N:25]1[C:18]([C:12]1[S:13][C:14]2[CH2:15][CH2:16][O:17][C:8]3[CH:7]=[C:6]([C:4]4[CH:5]=[N:1][NH:2][CH:3]=4)[CH:22]=[CH:21][C:9]=3[C:10]=2[N:11]=1)=[O:19]

Participants

3

Reactant 2

HCID 12012220(3S)-3-methylmorpholineHCID 582038838-(1H-Pyrazol-4-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid

Product 1

HCID 58203790HCID 58203790, compound

Procedure

Following the procedure for 103, 8-(1H-Pyrazol-4-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid (50.0 mg, 0.2 mmol) was reacted with (S)-3-methylmorpholine (1.2 equiv) to give 138 (14.9 mg, M+1 397.1)

Sources & evidence

ORD record
ord-98143546b6794361ac5b1e8314844e29
Source dataset
uspto-grants-2014_03
Patent number
US08673952B2

Reaction notes

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