HCID 42427166, compound → HCID 58203859, compound

HRID 1849146Notes

Reaction equation

HRID 1849146 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]([OH:20])=O)[S:13][C:14]=4[CH2:15][CH2:16][O:17][C:8]=3[CH:7]=2)[CH:3]=[N:2]1.[CH3:23][O:24][CH2:25][C@H:26]1[CH2:31][CH2:30][CH2:29][NH:28][CH2:27]1>>[CH3:23][O:24][CH2:25][C@@H:26]1[CH2:31][CH2:30][CH2:29][N:28]([C:18]([C:12]2[S:13][C:14]3[CH2:15][CH2:16][O:17][C:8]4[CH:7]=[C:6]([C:4]5[CH:3]=[N:2][NH:1][CH:5]=5)[CH:22]=[CH:21][C:9]=4[C:10]=3[N:11]=2)=[O:20])[CH2:27]1

Participants

3

Procedure

Following Example 216, to a well stirred solution of 8-(1H-Pyrazol-4-yl)-4,5-dihydro-6-oxa-3-thia-1-aza-benzo[e]azulene-2-carboxylic acid and (S)-3-(methoxymethyl)piperidine to give 223. MS: (ESI+)=425.1

Sources & evidence

ORD record
ord-c97a7d8482e54dde82702b5f52df0db9
Source dataset
uspto-grants-2015_02
Patent number
US08952043B2

Reaction notes

Loading…